[10-Q] Clene Inc. Quarterly Earnings Report
Clene Inc. is a clinical-stage pharmaceutical company developing clean-surfaced nanocrystal therapeutics for central nervous system disorders. For the quarter ended June 30, 2025, cash and cash equivalents were $7.3 million (down from $12.2 million at 12/31/2024), total assets were $22.1 million, and total liabilities were $30.7 million, producing a stockholders' deficit of $(8.6) million. Revenue remained minimal at $27 thousand for the quarter and $108 thousand for the six months ended June 30, 2025, while net loss for the six months was $8.17 million (net loss per share, basic and diluted, $0.89).
The company disclosed substantial doubt about its ability to continue as a going concern, citing recurring operating losses, negative operating cash flow of $9.8 million for the six months, and an accumulated deficit of $290.3 million. Material financing and liquidity items include a $45.1 million NIH grant with up to $30.9 million of subawards to Clene (reimbursements recognized; $6.4 million recognized in the six months), equity distribution proceeds of $5.1 million in the six months (plus $1.9 million subsequent to period end), and convertible senior secured notes with covenants requiring at least $2.0 million of unrestricted cash to avoid acceleration. Management is pursuing additional financing and has implemented cost-saving measures, but concluded these plans do not alleviate the substantial doubt about operations beyond one year.
Clene Inc. 猫 una societ脿 farmaceutica in fase clinica che sviluppa terapie a base di nanocristalli a superficie pulita per disturbi del sistema nervoso centrale. Nel trimestre chiuso al 30 giugno 2025, la liquidit脿 e gli equivalenti di cassa erano $7.3 million (in calo rispetto a $12.2 million al 31/12/2024), le attivit脿 totali ammontavano a $22.1 million e le passivit脿 totali a $30.7 million, generando un disavanzo patrimoniale di $(8.6) million. I ricavi sono rimasti ridotti, pari a $27 thousand nel trimestre e $108 thousand nei sei mesi chiusi al 30 giugno 2025; la perdita netta per i sei mesi 猫 stata di $8.17 million (perdita per azione, base e diluita, $0.89).
La societ脿 ha indicato di avere sostanziali dubbi sulla sua capacit脿 di continuare come azienda in attivit脿, citando perdite operative ricorrenti, un flusso di cassa operativo negativo di $9.8 million nei sei mesi e un deficit accumulato di $290.3 million. Tra gli elementi rilevanti per la liquidit脿 e il finanziamento figurano una $45.1 million NIH grant con fino a $30.9 million di subaward a Clene (rimborsi contabilizzati; $6.4 million riconosciuti nei sei mesi), proventi da emissione azionaria per $5.1 million nei sei mesi (pi霉 $1.9 million successivi alla chiusura del periodo) e note senior convertibili garantite con covenant che richiedono almeno $2.0 million di cassa non vincolata per evitare l'accelerazione. La direzione sta cercando finanziamenti aggiuntivi e ha attuato misure di contenimento dei costi, ma ha concluso che tali piani non eliminano i sostanziali dubbi sulla continuit脿 operativa oltre il prossimo anno.
Clene Inc. es una compa帽铆a farmac茅utica en fase cl铆nica que desarrolla terapias con nanocristales de superficie limpia para trastornos del sistema nervioso central. Para el trimestre concluido el 30 de junio de 2025, el efectivo y equivalentes de efectivo eran $7.3 million (desde $12.2 million al 31/12/2024), los activos totales eran $22.1 million y los pasivos totales $30.7 million, generando un d茅ficit de los accionistas de $(8.6) million. Los ingresos se mantuvieron m铆nimos en $27 thousand para el trimestre y $108 thousand para los seis meses cerrados el 30 de junio de 2025; la p茅rdida neta en los seis meses fue de $8.17 million (p茅rdida por acci贸n, b谩sica y diluida, $0.89).
La empresa declar贸 tener dudas sustanciales sobre su capacidad para continuar como empresa en funcionamiento, citando p茅rdidas operativas recurrentes, flujo de efectivo operativo negativo de $9.8 million en los seis meses y un d茅ficit acumulado de $290.3 million. Entre los elementos materiales de financiaci贸n y liquidez se incluyen una $45.1 million NIH grant con hasta $30.9 million en subawards a Clene (reembolsos reconocidos; $6.4 million reconocidos en los seis meses), ingresos por colocaci贸n de acciones por $5.1 million en los seis meses (m谩s $1.9 million posteriores al cierre del periodo) y pagar茅s convertibles senior garantizados con convenios que exigen al menos $2.0 million de efectivo no restringido para evitar la aceleraci贸n. La direcci贸n est谩 buscando financiaci贸n adicional y ha implementado medidas de ahorro, pero concluy贸 que estos planes no eliminan la duda sustancial sobre la continuidad m谩s all谩 de un a帽o.
Clene Inc.電� 欷戩稊鞁犼步瓿� 歆堩櫂鞚� 雽�靸侅溂搿� 旯仐頃� 響滊┐鞚� 雮橂吀瓴办爼(雮橂吀韥Μ鞀ろ儓) 旃橂鞝滊ゼ 臧滊皽頃橂姅 鞛勳儊 雼硠 鞝滌暯須岇偓鞛呺媹雼�. 2025雲� 6鞗� 30鞚茧 膦呺霅� 攵勱赴 旮办 順勱笀 氚� 順勱笀靹膘瀽靷办潃 $7.3 million (2024雲� 12鞗� 31鞚检潣 $12.2 million鞐愳劀 臧愳唽), 齑濎瀽靷办潃 $22.1 million, 齑濍秬毂勲姅 $30.7 million鞙茧 欤检＜歆�攵勳澊 $(8.6) million鞚� 鞝侅瀽毳� 旮半頄堨姷雼堧嫟. 攵勱赴 毵れ稖鞚� $27 thousand, 6臧滌洈 雸勳爜 毵れ稖鞚� $108 thousand鞙茧 氙鸽頄堨溂氅�, 6臧滌洈 靾滌啇鞁れ潃 $8.17 million (欤茧嫻靾滌啇鞁� 旮半掣 氚� 頋劃 $0.89)鞓赌鞀惦媹雼�.
须岇偓电� 瓿勳啀旮办梾鞙茧靹滌潣 臁挫啀 電ル牓鞐� 雽�頃� 欷戨寑頃� 鞚橂鞚� 鞛堧嫟瓿� 瓿奠嫓頄堨溂氅�, 氚橂车霅橂姅 鞓侅梾靻愳嫟, 6臧滌洈臧� $9.8 million鞚� 鞓侅梾頇滊彊鞙茧 鞚疙暅 順勱笀頋愲 鞚岇垬, 雸勳爜瓴办啇旮� $290.3 million鞚� 攴缄卑搿� 霌れ棃鞀惦媹雼�. 欤检殧 鞛愱笀 氚� 鞙犽彊靹� 頃鞙茧電� 韥措爩鞐� 雽�頃� 斓滊寑 $30.9 million鞚� 頃橃渼靾橃棳(subaward)毳� 韽暔頃橂姅 $45.1 million NIH grant (頇橁笁 鞚胳嫕; 6臧滌洈 霃欖晥 $6.4 million 鞚胳嫕), 6臧滌洈 霃欖晥鞚� 欤检嫕 氚半秳 靾橃澋 $5.1 million (旮瓣皠 鞚错泟 $1.9 million 於旉皜) 氚� 臧�靻嶍檾毳� 頂柬晿霠る┐ 斓滌唽頃� $2.0 million鞚� 氍挫牅頃� 順勱笀鞚� 氤挫湢頃橂弰搿� 鞖旉惮頃橂姅 鞎届爼鞚� 鞛堧姅 雼措炒攵� 靹犾垳鞙� 鞝勴櫂毂勱秾 霌膘澊 韽暔霅╇媹雼�. 瓴届榿歆勳潃 於旉皜 鞛愱笀 臁半嫭鞚� 氇儔頃橁碃 牍勳毄 鞝堦皭 臁办箻毳� 鞁滍枆頃橁碃 鞛堨溂雮�, 鞚措摛 瓿勴殟毵岇溂搿滊姅 頄ロ泟 1雲勳潉 雱橁波 瓿勳啀旮办梾鞙茧靹滌潣 欷戨寑頃� 鞚橂鞚� 頃挫唽頃� 靾� 鞐嗠嫟瓿� 瓴半歆�鞐堨姷雼堧嫟.
Clene Inc. est une soci茅t茅 pharmaceutique en phase clinique qui d茅veloppe des th茅rapeutiques 脿 base de nanocristaux 脿 surface propre pour les troubles du syst猫me nerveux central. Pour le trimestre clos le 30 juin 2025, la tr茅sorerie et 茅quivalents de tr茅sorerie s鈥櫭﹍evaient 脿 $7.3 million (en baisse par rapport 脿 $12.2 million au 31/12/2024), l鈥檃ctif total 茅tait de $22.1 million et le passif total de $30.7 million, g茅n茅rant un d茅ficit des actionnaires de $(8.6) million. Les revenus sont rest茅s minimaux, 脿 $27 thousand pour le trimestre et $108 thousand pour les six mois clos le 30 juin 2025; la perte nette pour les six mois s鈥檈st 茅lev茅e 脿 $8.17 million (perte par action, de base et dilu茅e, $0.89).
La soci茅t茅 a d茅clar茅 avoir un doute important quant 脿 sa capacit茅 脿 poursuivre son exploitation, invoquant des pertes d鈥檈xploitation r茅currentes, un flux de tr茅sorerie op茅rationnel n茅gatif de $9.8 million sur six mois et un d茅ficit cumul茅 de $290.3 million. Les 茅l茅ments significatifs en mati猫re de financement et de liquidit茅 incluent une $45.1 million NIH grant avec jusqu鈥櫭� $30.9 million de sous-attributions 脿 Clene (remboursements comptabilis茅s; $6.4 million comptabilis茅s sur les six mois), des produits d鈥櫭﹎ission d鈥檃ctions de $5.1 million au cours des six mois (plus $1.9 million apr猫s la cl么ture de la p茅riode) et des obligations senior convertibles garanties comportant des covenants exigeant au moins $2.0 million de tr茅sorerie non restreinte pour 茅viter l鈥檈xigibilit茅 anticip茅e. La direction recherche des financements additionnels et a mis en place des mesures de r茅duction des co没ts, mais conclut que ces plans n鈥櫭ヽartent pas le doute important sur la continuit茅 d鈥檈xploitation au鈥慸el脿 d鈥檜n an.
Clene Inc. ist ein forschungsaktives Pharmaunternehmen in der klinischen Entwicklungsphase, das 鈥瀋lean-surfaced鈥� Nanokristall-Therapeutika f眉r Erkrankungen des zentralen Nervensystems entwickelt. Zum Quartalsende 30. Juni 2025 beliefen sich die liquiden Mittel und Zahlungsmittel盲quivalente auf $7.3 million (R眉ckgang gegen眉ber $12.2 million zum 31.12.2024), die Gesamtverm枚genswerte auf $22.1 million und die Gesamtverbindlichkeiten auf $30.7 million, was zu einem Eigenkapitalfehlbetrag von $(8.6) million f眉hrte. Die Umsatzerl枚se blieben mit $27 thousand im Quartal und $108 thousand in den sechs Monaten zum 30. Juni 2025 gering; der Nettoverlust f眉r die sechs Monate betrug $8.17 million (Ergebnis je Aktie, unverw盲ssert und verw盲ssert, $0.89).
Das Unternehmen 盲u脽erte
- None.
- None.
Insights
TL;DR: Cash has declined to $7.3M, burn remains high, NIH grant provides material support, but going-concern risk persists.
Clene's operating profile shows minimal commercial revenue and continued R&D expense driving a six-month net loss of $8.17M. The company recognized $6.4M of NIH-related reimbursements in the period, which materially offset R&D expense but are reimbursement-based rather than recurring product sales. Operating cash outflow of $9.8M and a decline in cash from $12.2M to $7.3M indicate near-term financing needs. The $10.0M senior secured convertible notes and related derivative features create dilution and contingent liabilities; the SSCP note covenant to maintain $2.0M unrestricted cash is a near-term liquidity threshold. Overall, the filing is materially negative for equity holders absent committed financing.
TL;DR: Strong grant support and recent equity raises help near-term funding, but debt covenants and stockholder deficit raise governance and liquidity concerns.
The NIH award and $5.1M of ATM proceeds in the six months are tangible financing accomplishments that reduce near-term cash pressure and support clinical programs. However, significant derivative and warrant liabilities, convertible note conversion features, and contingent SSCPN fees and registration penalties pose execution and shareholder dilution risks. The company discloses that implemented cost controls are insufficient to remove substantial doubt about going concern, signaling elevated financing and governance risk until longer-term funding or licensing/collaboration agreements are secured.
Clene Inc. 猫 una societ脿 farmaceutica in fase clinica che sviluppa terapie a base di nanocristalli a superficie pulita per disturbi del sistema nervoso centrale. Nel trimestre chiuso al 30 giugno 2025, la liquidit脿 e gli equivalenti di cassa erano $7.3 million (in calo rispetto a $12.2 million al 31/12/2024), le attivit脿 totali ammontavano a $22.1 million e le passivit脿 totali a $30.7 million, generando un disavanzo patrimoniale di $(8.6) million. I ricavi sono rimasti ridotti, pari a $27 thousand nel trimestre e $108 thousand nei sei mesi chiusi al 30 giugno 2025; la perdita netta per i sei mesi 猫 stata di $8.17 million (perdita per azione, base e diluita, $0.89).
La societ脿 ha indicato di avere sostanziali dubbi sulla sua capacit脿 di continuare come azienda in attivit脿, citando perdite operative ricorrenti, un flusso di cassa operativo negativo di $9.8 million nei sei mesi e un deficit accumulato di $290.3 million. Tra gli elementi rilevanti per la liquidit脿 e il finanziamento figurano una $45.1 million NIH grant con fino a $30.9 million di subaward a Clene (rimborsi contabilizzati; $6.4 million riconosciuti nei sei mesi), proventi da emissione azionaria per $5.1 million nei sei mesi (pi霉 $1.9 million successivi alla chiusura del periodo) e note senior convertibili garantite con covenant che richiedono almeno $2.0 million di cassa non vincolata per evitare l'accelerazione. La direzione sta cercando finanziamenti aggiuntivi e ha attuato misure di contenimento dei costi, ma ha concluso che tali piani non eliminano i sostanziali dubbi sulla continuit脿 operativa oltre il prossimo anno.
Clene Inc. es una compa帽铆a farmac茅utica en fase cl铆nica que desarrolla terapias con nanocristales de superficie limpia para trastornos del sistema nervioso central. Para el trimestre concluido el 30 de junio de 2025, el efectivo y equivalentes de efectivo eran $7.3 million (desde $12.2 million al 31/12/2024), los activos totales eran $22.1 million y los pasivos totales $30.7 million, generando un d茅ficit de los accionistas de $(8.6) million. Los ingresos se mantuvieron m铆nimos en $27 thousand para el trimestre y $108 thousand para los seis meses cerrados el 30 de junio de 2025; la p茅rdida neta en los seis meses fue de $8.17 million (p茅rdida por acci贸n, b谩sica y diluida, $0.89).
La empresa declar贸 tener dudas sustanciales sobre su capacidad para continuar como empresa en funcionamiento, citando p茅rdidas operativas recurrentes, flujo de efectivo operativo negativo de $9.8 million en los seis meses y un d茅ficit acumulado de $290.3 million. Entre los elementos materiales de financiaci贸n y liquidez se incluyen una $45.1 million NIH grant con hasta $30.9 million en subawards a Clene (reembolsos reconocidos; $6.4 million reconocidos en los seis meses), ingresos por colocaci贸n de acciones por $5.1 million en los seis meses (m谩s $1.9 million posteriores al cierre del periodo) y pagar茅s convertibles senior garantizados con convenios que exigen al menos $2.0 million de efectivo no restringido para evitar la aceleraci贸n. La direcci贸n est谩 buscando financiaci贸n adicional y ha implementado medidas de ahorro, pero concluy贸 que estos planes no eliminan la duda sustancial sobre la continuidad m谩s all谩 de un a帽o.
Clene Inc.電� 欷戩稊鞁犼步瓿� 歆堩櫂鞚� 雽�靸侅溂搿� 旯仐頃� 響滊┐鞚� 雮橂吀瓴办爼(雮橂吀韥Μ鞀ろ儓) 旃橂鞝滊ゼ 臧滊皽頃橂姅 鞛勳儊 雼硠 鞝滌暯須岇偓鞛呺媹雼�. 2025雲� 6鞗� 30鞚茧 膦呺霅� 攵勱赴 旮办 順勱笀 氚� 順勱笀靹膘瀽靷办潃 $7.3 million (2024雲� 12鞗� 31鞚检潣 $12.2 million鞐愳劀 臧愳唽), 齑濎瀽靷办潃 $22.1 million, 齑濍秬毂勲姅 $30.7 million鞙茧 欤检＜歆�攵勳澊 $(8.6) million鞚� 鞝侅瀽毳� 旮半頄堨姷雼堧嫟. 攵勱赴 毵れ稖鞚� $27 thousand, 6臧滌洈 雸勳爜 毵れ稖鞚� $108 thousand鞙茧 氙鸽頄堨溂氅�, 6臧滌洈 靾滌啇鞁れ潃 $8.17 million (欤茧嫻靾滌啇鞁� 旮半掣 氚� 頋劃 $0.89)鞓赌鞀惦媹雼�.
须岇偓电� 瓿勳啀旮办梾鞙茧靹滌潣 臁挫啀 電ル牓鞐� 雽�頃� 欷戨寑頃� 鞚橂鞚� 鞛堧嫟瓿� 瓿奠嫓頄堨溂氅�, 氚橂车霅橂姅 鞓侅梾靻愳嫟, 6臧滌洈臧� $9.8 million鞚� 鞓侅梾頇滊彊鞙茧 鞚疙暅 順勱笀頋愲 鞚岇垬, 雸勳爜瓴办啇旮� $290.3 million鞚� 攴缄卑搿� 霌れ棃鞀惦媹雼�. 欤检殧 鞛愱笀 氚� 鞙犽彊靹� 頃鞙茧電� 韥措爩鞐� 雽�頃� 斓滊寑 $30.9 million鞚� 頃橃渼靾橃棳(subaward)毳� 韽暔頃橂姅 $45.1 million NIH grant (頇橁笁 鞚胳嫕; 6臧滌洈 霃欖晥 $6.4 million 鞚胳嫕), 6臧滌洈 霃欖晥鞚� 欤检嫕 氚半秳 靾橃澋 $5.1 million (旮瓣皠 鞚错泟 $1.9 million 於旉皜) 氚� 臧�靻嶍檾毳� 頂柬晿霠る┐ 斓滌唽頃� $2.0 million鞚� 氍挫牅頃� 順勱笀鞚� 氤挫湢頃橂弰搿� 鞖旉惮頃橂姅 鞎届爼鞚� 鞛堧姅 雼措炒攵� 靹犾垳鞙� 鞝勴櫂毂勱秾 霌膘澊 韽暔霅╇媹雼�. 瓴届榿歆勳潃 於旉皜 鞛愱笀 臁半嫭鞚� 氇儔頃橁碃 牍勳毄 鞝堦皭 臁办箻毳� 鞁滍枆頃橁碃 鞛堨溂雮�, 鞚措摛 瓿勴殟毵岇溂搿滊姅 頄ロ泟 1雲勳潉 雱橁波 瓿勳啀旮办梾鞙茧靹滌潣 欷戨寑頃� 鞚橂鞚� 頃挫唽頃� 靾� 鞐嗠嫟瓿� 瓴半歆�鞐堨姷雼堧嫟.
Clene Inc. est une soci茅t茅 pharmaceutique en phase clinique qui d茅veloppe des th茅rapeutiques 脿 base de nanocristaux 脿 surface propre pour les troubles du syst猫me nerveux central. Pour le trimestre clos le 30 juin 2025, la tr茅sorerie et 茅quivalents de tr茅sorerie s鈥櫭﹍evaient 脿 $7.3 million (en baisse par rapport 脿 $12.2 million au 31/12/2024), l鈥檃ctif total 茅tait de $22.1 million et le passif total de $30.7 million, g茅n茅rant un d茅ficit des actionnaires de $(8.6) million. Les revenus sont rest茅s minimaux, 脿 $27 thousand pour le trimestre et $108 thousand pour les six mois clos le 30 juin 2025; la perte nette pour les six mois s鈥檈st 茅lev茅e 脿 $8.17 million (perte par action, de base et dilu茅e, $0.89).
La soci茅t茅 a d茅clar茅 avoir un doute important quant 脿 sa capacit茅 脿 poursuivre son exploitation, invoquant des pertes d鈥檈xploitation r茅currentes, un flux de tr茅sorerie op茅rationnel n茅gatif de $9.8 million sur six mois et un d茅ficit cumul茅 de $290.3 million. Les 茅l茅ments significatifs en mati猫re de financement et de liquidit茅 incluent une $45.1 million NIH grant avec jusqu鈥櫭� $30.9 million de sous-attributions 脿 Clene (remboursements comptabilis茅s; $6.4 million comptabilis茅s sur les six mois), des produits d鈥櫭﹎ission d鈥檃ctions de $5.1 million au cours des six mois (plus $1.9 million apr猫s la cl么ture de la p茅riode) et des obligations senior convertibles garanties comportant des covenants exigeant au moins $2.0 million de tr茅sorerie non restreinte pour 茅viter l鈥檈xigibilit茅 anticip茅e. La direction recherche des financements additionnels et a mis en place des mesures de r茅duction des co没ts, mais conclut que ces plans n鈥櫭ヽartent pas le doute important sur la continuit茅 d鈥檈xploitation au鈥慸el脿 d鈥檜n an.
Clene Inc. ist ein forschungsaktives Pharmaunternehmen in der klinischen Entwicklungsphase, das 鈥瀋lean-surfaced鈥� Nanokristall-Therapeutika f眉r Erkrankungen des zentralen Nervensystems entwickelt. Zum Quartalsende 30. Juni 2025 beliefen sich die liquiden Mittel und Zahlungsmittel盲quivalente auf $7.3 million (R眉ckgang gegen眉ber $12.2 million zum 31.12.2024), die Gesamtverm枚genswerte auf $22.1 million und die Gesamtverbindlichkeiten auf $30.7 million, was zu einem Eigenkapitalfehlbetrag von $(8.6) million f眉hrte. Die Umsatzerl枚se blieben mit $27 thousand im Quartal und $108 thousand in den sechs Monaten zum 30. Juni 2025 gering; der Nettoverlust f眉r die sechs Monate betrug $8.17 million (Ergebnis je Aktie, unverw盲ssert und verw盲ssert, $0.89).
Das Unternehmen 盲u脽erte
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
(Mark One)
For the quarterly period ended
or
For the transition period from _____________ to _____________
Commission file number:
CLENE INC.
(Exact name of registrant as specified in its charter)
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(Registrant’s telephone number, including area code)
| N/A |
(Former name, former address, and former fiscal year, if changed since last report)
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered | ||
| | | The | ||
| | | The |
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
| Large accelerated filer | ☐ | Accelerated filer | ☐ |
| | ☒ | Smaller reporting company | |
| Emerging growth company | |
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes
The number of shares outstanding of the Registrant’s common stock as of August 11, 2025 was
CLENE INC.
Quarterly Report on Form 10-Q for the Quarter Ended June 30, 2025
| PART I—FINANCIAL INFORMATION | 1 |
||
| Item 1. |
Financial Statements (Unaudited) |
1 |
|
| Condensed Consolidated Balance Sheets |
1 | ||
| Condensed Consolidated Statements of Operations and Comprehensive Loss |
2 | ||
| Condensed Consolidated Statements of Stockholders’ Equity (Deficit) |
3 |
||
| Condensed Consolidated Statements of Cash Flows |
4 |
||
| Notes to Condensed Consolidated Financial Statements |
5 |
||
| Item 2. |
Management’s Discussion and Analysis of Financial Condition and Results of Operations |
30 |
|
| Item 3. |
Quantitative and Qualitative Disclosures About Market Risk |
44 |
|
| Item 4. |
Controls and Procedures |
44 |
|
| PART II—OTHER INFORMATION |
46 |
||
| Item 1. |
Legal Proceedings |
46 |
|
| Item 1A. |
Risk Factors |
46 |
|
| Item 2. |
Unregistered Sales of Equity Securities and Use of Proceeds |
46 |
|
| Item 3. |
Defaults Upon Senior Securities |
46 |
|
| Item 4. |
Mine Safety Disclosures |
46 |
|
| Item 5. |
Other Information |
46 |
|
| Item 6. |
Exhibits |
47 |
|
PART I—FINANCIAL INFORMATION
Item 1. Financial Statements
CLENE INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except share and per share amounts)
(Unaudited)
| June 30, | December 31, | |||||||
| 2025 | 2024 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | $ | ||||||
| Accounts receivable | ||||||||
| Inventory | ||||||||
| Prepaid expenses and other current assets | ||||||||
| Total current assets | ||||||||
| Restricted cash | ||||||||
| Operating lease right-of-use assets | ||||||||
| Property and equipment, net | ||||||||
| TOTAL ASSETS | $ | $ | ||||||
| LIABILITIES AND STOCKHOLDERS’ DEFICIT | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | $ | ||||||
| Accrued liabilities | ||||||||
| Operating lease obligations, current portion | ||||||||
| Notes payable, current portion | ||||||||
| Total current liabilities | ||||||||
| Operating lease obligations, net of current portion | ||||||||
| Notes payable, net of current portion | ||||||||
| Convertible notes payable | ||||||||
| Common stock warrant liabilities | ||||||||
| Derivative liabilities | ||||||||
| TOTAL LIABILITIES | ||||||||
| Commitments and contingencies (Note 9) | ||||||||
| Stockholders’ deficit: | ||||||||
| Common stock, $ par value: shares authorized; and shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively | ||||||||
| Additional paid-in capital | ||||||||
| Accumulated deficit | ( | ) | ( | ) | ||||
| Accumulated other comprehensive income | ||||||||
| TOTAL STOCKHOLDERS’ DEFICIT | ( | ) | ( | ) | ||||
| TOTAL LIABILITIES AND STOCKHOLDERS’ DEFICIT | $ | $ | ||||||
See accompanying notes to the condensed consolidated financial statements.
CLENE INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(In thousands, except share and per share amounts)
(Unaudited)
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| 2025 |
2024 |
2025 |
2024 |
|||||||||||||
| Revenue: |
||||||||||||||||
| Product revenue |
$ | $ | $ | $ | ||||||||||||
| Royalty revenue |
||||||||||||||||
| Total revenue |
||||||||||||||||
| Operating expenses: |
||||||||||||||||
| Cost of revenue |
||||||||||||||||
| Research and development |
||||||||||||||||
| General and administrative |
||||||||||||||||
| Total operating expenses |
||||||||||||||||
| Loss from operations |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Other income (expense), net: |
||||||||||||||||
| Interest income |
||||||||||||||||
| Interest expense |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Change in fair value of common stock warrant liabilities |
( |
) | ||||||||||||||
| Change in fair value of derivative liabilities |
( |
) | ||||||||||||||
| Change in fair value of Clene Nanomedicine contingent earn-out liability |
||||||||||||||||
| Change in fair value of Initial Stockholders contingent earn-out liability |
||||||||||||||||
| Research and development tax credits and unrestricted grants |
||||||||||||||||
| Total other income (expense), net |
( |
) | ( |
) | ||||||||||||
| Net loss before income taxes |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Income tax expense |
||||||||||||||||
| Net loss |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Other comprehensive income (loss): |
||||||||||||||||
| Unrealized loss on available-for-sale securities |
$ | $ | $ | $ | ( |
) | ||||||||||
| Foreign currency translation adjustments |
( |
) | ||||||||||||||
| Total other comprehensive income (loss) |
( |
) | ||||||||||||||
| Comprehensive loss |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Net loss per share – basic and diluted |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Weighted average common shares used to compute basic and diluted net loss per share |
||||||||||||||||
See accompanying notes to the condensed consolidated financial statements.
CLENE INC.
CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY (DEFICIT)
(In thousands, except share amounts)
(Unaudited
| Common Stock |
Additional Paid-In Capital |
Accumulated Deficit |
Accumulated Other Comprehensive Income (Loss) |
Total Stockholders’ Equity (Deficit) |
||||||||||||||||||||
| Shares |
Amount |
|||||||||||||||||||||||
| Balances at December 31, 2024 |
$ | $ | $ | ( |
) | $ | $ | ( |
) | |||||||||||||||
| Issuance of common stock |
||||||||||||||||||||||||
| Stock-based compensation expense |
— | |||||||||||||||||||||||
| Foreign currency translation adjustment |
— | |||||||||||||||||||||||
| Net loss |
— | ( |
) | ( |
) | |||||||||||||||||||
| Balances at March 31, 2025 |
$ | $ | $ | ( |
) | $ | $ | ( |
) | |||||||||||||||
| Issuance of common stock |
||||||||||||||||||||||||
| Stock-based compensation expense |
— | |||||||||||||||||||||||
| Foreign currency translation adjustment |
— | |||||||||||||||||||||||
| Net loss |
— | ( |
) | ( |
) | |||||||||||||||||||
| Balances at June 30, 2025 |
$ | $ | $ | ( |
) | $ | $ | ( |
) | |||||||||||||||
| Balances at December 31, 2023 |
( |
) | ||||||||||||||||||||||
| Stock-based compensation expense |
— | |||||||||||||||||||||||
| Issuance of common stock upon vesting of restricted stock awards |
||||||||||||||||||||||||
| Unrealized loss on available-for-sale securities |
— | ( |
) | ( |
) | |||||||||||||||||||
| Foreign currency translation adjustment |
— | ( |
) | ( |
) | |||||||||||||||||||
| Net loss |
— | ( |
) | ( |
) | |||||||||||||||||||
| Balances at March 31, 2024 |
$ | $ | $ | ( |
) | $ | $ | |||||||||||||||||
| Exercise of stock options |
||||||||||||||||||||||||
| Stock-based compensation expense |
— | |||||||||||||||||||||||
| Unrealized gain on available-for-sale securities |
— | |||||||||||||||||||||||
| Foreign currency translation adjustment |
— | |||||||||||||||||||||||
| Net loss |
— | ( |
) | ( |
) | |||||||||||||||||||
| Balances at June 30, 2024 |
$ | $ | $ | ( |
) | $ | $ | ( |
) | |||||||||||||||
See accompanying notes to the condensed consolidated financial statements.
CLENE INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(In thousands)
(Unaudited)
| Six Months Ended June 30, |
||||||||
| 2025 |
2024 |
|||||||
| Cash flows from operating activities: |
||||||||
| Net loss |
$ | ( |
) | $ | ( |
) | ||
| Adjustments to reconcile net loss to net cash used in operating activities: |
||||||||
| Depreciation |
||||||||
| Non-cash lease expense |
||||||||
| Issuance of common stock as payment of outstanding indebtedness |
||||||||
| Change in fair value of common stock warrant liabilities |
( |
) | ( |
) | ||||
| Change in fair value of derivative liabilities |
( |
) | ||||||
| Change in fair value of Clene Nanomedicine contingent earn-out liability |
( |
) | ||||||
| Change in fair value of Initial Stockholders contingent earn-out liability |
( |
) | ||||||
| Stock-based compensation expense |
||||||||
| Accretion of debt discount |
||||||||
| Non-cash interest income on marketable securities |
( |
) | ||||||
| Non-cash interest expense on notes payable |
||||||||
| Changes in operating assets and liabilities: |
||||||||
| Accounts receivable |
||||||||
| Inventory |
( |
) | ||||||
| Prepaid expenses and other current assets |
( |
) | ( |
) | ||||
| Accounts payable |
( |
) | ( |
) | ||||
| Accrued liabilities |
( |
) | ||||||
| Operating lease obligations |
( |
) | ( |
) | ||||
| Net cash used in operating activities |
( |
) | ( |
) | ||||
| Cash flows from investing activities: |
||||||||
| Purchases of marketable securities |
( |
) | ||||||
| Proceeds from maturities of marketable securities |
||||||||
| Purchases of property and equipment |
( |
) | ||||||
| Net cash provided by investing activities |
||||||||
| Cash flows from financing activities: |
||||||||
| Proceeds from exercise of stock options |
||||||||
| Proceeds from issuance of common stock, net of offering costs |
||||||||
| Payments of notes payable |
( |
) | ||||||
| Payments of finance lease obligations |
( |
) | ||||||
| Net cash provided by financing activities |
||||||||
| Effect of foreign exchange rate changes on cash and restricted cash |
( |
) | ||||||
| Net decrease in cash, cash equivalents and restricted cash |
( |
) | ( |
) | ||||
| Cash, cash equivalents and restricted cash – beginning of period |
||||||||
| Cash, cash equivalents and restricted cash – end of period |
$ | $ | ||||||
| Reconciliation of cash, cash equivalents and restricted cash to the consolidated balance sheets: |
||||||||
| Cash and cash equivalents |
$ | $ | ||||||
| Restricted cash |
||||||||
| Cash, cash equivalents and restricted cash |
$ | $ | ||||||
| Supplemental disclosure of non-cash investing and financing activities: |
||||||||
| Issuance of common stock as payment of outstanding indebtedness |
$ | $ | ||||||
| Supplemental cash flow information: |
||||||||
| Cash paid for interest expense |
$ | $ | ||||||
See accompanying notes to the condensed consolidated financial statements.
CLENE INC.
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(Unaudited)
Note 1. Nature of the Business
Clene Inc. (the “Company,” “we,” “us,” or similar such references) is a clinical-stage pharmaceutical company pioneering the discovery, development, and commercialization of novel clean-surfaced nanotechnology therapeutics. We have developed an electro-crystal-chemistry drug development platform that enables production of concentrated, stable, highly active, clean-surfaced nanocrystal suspensions. We have multiple drug assets currently in development for applications primarily in neurology. Our efforts are currently focused on addressing the high unmet medical needs in central nervous system disorders including amyotrophic lateral sclerosis (“ALS”), multiple sclerosis (“MS”), and Parkinson’s disease (“PD”). Our patented electro-crystal-chemistry manufacturing platform further enables us to develop very low concentration dietary supplements to advance the health and well-being of broad populations. These dietary supplements can vary greatly and include nanocrystals of varying composition, shapes and sizes as well as ionic solutions with diverse metallic constituents. Dietary supplements are marketed and distributed through our wholly owned subsidiary, dOrbital, Inc., or through an exclusive license with 4Life Research LLC (“4Life”), an international supplier of health supplements, stockholder, and related party (see Note 15).
We became a public company on December 30, 2020 (the “Closing Date”) when we completed a reverse recapitalization (the “Reverse Recapitalization”) with Tottenham Acquisition I Limited (“Tottenham”), Tottenham’s wholly-owned subsidiary, Chelsea Worldwide Inc., and Creative Worldwide Inc., a wholly-owned subsidiary of Chelsea Worldwide Inc. On the Closing Date, Chelsea Worldwide Inc. changed its name to Clene Inc. and listed its shares of common stock, par value $
Going Concern
We incurred a loss from operations of $
We have incurred significant losses and negative cash flows from operations since our inception. We have not generated significant revenues since our inception, and we do not anticipate generating significant revenues unless we successfully complete development and obtain regulatory approval for commercialization of a drug candidate. We expect to incur additional losses in the future, particularly as we advance the development of our clinical-stage drug candidates, continue research and development of our preclinical drug candidates, and initiate additional clinical trials of, and seek regulatory approval for, these and other future drug candidates. We expect that within the next twelve months, we will not have sufficient cash and other resources on hand to sustain our current operations or meet our obligations as they become due unless we obtain additional financing. Additionally, pursuant to our senior secured convertible promissory notes (the “2024 SSCP Notes”), we are required to maintain unrestricted cash and cash equivalents of at least $
To mitigate our funding needs, we plan to raise additional funding, including exploring equity financing and offerings, debt financing, licensing or collaboration arrangements with third parties, as well as utilizing our existing at-the-market facility and equity purchase agreement and potential proceeds from the exercise of outstanding warrants and stock options. These plans are subject to market conditions and reliance on third parties, and there is no assurance that effective implementation of our plans will result in the necessary funding to continue current operations. During the three and six months ended June 30, 2025, we generated $
The accompanying condensed consolidated financial statements have been prepared assuming we will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. As a result, the accompanying condensed consolidated financial statements do not include any adjustments relating to the recoverability and classification of assets and their carrying amounts, or the amounts and classification of liabilities that may result should we be unable to continue as a going concern.
Note 2. Summary of Significant Accounting Policies
Basis of Presentation
The accompanying condensed consolidated financial statements include the accounts of Clene Inc. and our wholly-owned subsidiaries, Clene Nanomedicine, Inc., a subsidiary incorporated in Delaware, Clene Australia Pty Ltd (“Clene Australia”), a subsidiary incorporated in Australia, Clene Netherlands B.V. (“Clene Netherlands”), a subsidiary incorporated in the Netherlands, and dOrbital, Inc., a subsidiary incorporated in Delaware, after elimination of all intercompany accounts and transactions. We have prepared the accompanying condensed consolidated financial statements in accordance with United States (“U.S.”) Generally Accepted Accounting Principles (“GAAP”) for interim financial reporting and as required by Regulation S-X, Rule 10-01. The condensed consolidated financial statements have been prepared on the same basis as our audited annual consolidated financial statements and, in the opinion of management, reflect all adjustments, which are normal and recurring in nature, necessary for fair financial statement presentation. The financial data and other information disclosed in the condensed consolidated financial statements and related notes for the three and six months ended June 30, 2025 and 2024 are unaudited.
Results of operations for the three and six months ended June 30, 2025 and 2024 are not necessarily indicative of the results for the entire fiscal year or any other period. The condensed consolidated financial statements for the three and six months ended June 30, 2025 and 2024 should be read in conjunction with the audited consolidated financial statements included in our Annual Report on Form 10-K.
Reverse Stock Split
Effective July 11, 2024 (the “Effective Date”), we filed a Certificate of Amendment to our Fourth Amended and Restated Certificate of Incorporation with the Secretary of State of the State of Delaware, to effect a 1-for-
The Reverse Stock Split did not reduce the total number of authorized shares of Common Stock or preferred stock, par value $
Use of Estimates
The preparation of condensed consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets, liabilities, and disclosure of contingent assets and liabilities, and the reported amounts of expenses. We base our estimates on historical experience and various other assumptions that we believe to be reasonable. Actual results may differ from those estimates or assumptions. Estimates are periodically reviewed in light of changes in circumstances, facts, and experience, and any changes in estimates will be recorded in future periods as they develop.
Risks and Uncertainties
We are subject to certain risks and uncertainties and believe that changes in any of the following areas could have a material adverse effect on future financial condition, results of operations, or cash flows: ability to obtain additional financing; regulatory approval and market acceptance of, and reimbursement for, product candidates; performance of third-party contract research organizations (“CROs”) and manufacturers upon which we rely; protection of our intellectual property; litigation or claims against us based on intellectual property, patent, product, regulatory, or other factors; and our ability to attract and retain employees necessary to support our growth. The product candidates we develop require approvals from regulatory agencies prior to commercial sales. There can be no assurance that our current and future product candidates will receive the necessary approvals or be commercially successful. If we are denied approval or approval is delayed, it will have a material adverse impact on our business and our condensed consolidated financial statements.
Concentrations of Credit Risk
Financial instruments that potentially subject us to significant concentrations of credit risk consist primarily of cash. Our cash is held in financial institutions and amounts on deposit may at times exceed federally insured limits. We have not experienced any losses on our deposits of cash and do not believe that we are subject to unusual credit risk beyond the normal credit risk associated with commercial banking relationships.
Cash and Cash Equivalents
We consider all short-term investments with original maturities of 90 days or less when purchased to be cash equivalents.
Restricted Cash
We classify cash as restricted when it is unavailable for withdrawal or use in our general operating activities. Restricted cash is classified as current and noncurrent on the condensed consolidated balance sheets based on the nature of the restriction. Our restricted cash balance includes contractually restricted deposits related to our corporate credit card.
Inventory
Inventory is stated at historic cost on a first-in first-out basis. Our inventory consisted of $
Property and Equipment
Property and equipment are stated at cost less accumulated depreciation. Property and equipment consist of laboratory and office equipment, computer software, and leasehold improvements. Depreciation is calculated using the straight-line method over the estimated economic useful lives of the assets, which are
We capitalize costs to obtain or develop computer software for internal use, including development costs incurred during the software development stage and costs to obtain software for access and conversion of historical data. We also capitalize costs to modify, upgrade, or enhance existing internal-use software that result in additional functionality. We expense costs incurred during the preliminary project stage, training costs, data conversion costs, and maintenance costs.
Debt
When debt is issued and a derivative is required to be separated (e.g., bifurcated conversion option) or another separate freestanding financial instrument (e.g., warrant) is issued, costs and fees incurred are allocated to the instruments issued (or bifurcated) in proportion to the allocation of proceeds. When some portions of the costs and fees relate to a bifurcated derivative or freestanding financial instrument that is being subsequently measured at fair value, those allocated costs are expensed immediately. Debt discounts, debt premiums, and debt issuance costs related to debt are recorded as deductions that net against the principal value of the debt and are amortized to interest expense over the contractual term of the debt using the effective interest method.
In accordance with ASC 470-20, Debt with Conversion and Other Options, when we issue debt with warrants, we treat the warrants as a debt discount, recorded as a contra-liability against the debt, and amortize the balance over the life of the underlying debt as interest expense in the condensed consolidated statements of operations and comprehensive loss. The offset to the contra-liability is recorded as additional paid-in capital in the condensed consolidated balance sheets if the warrants are not treated as a derivative or liability under ASC 480, Distinguishing Liabilities from Equity (“ASC 480”). Otherwise, the offset to the contra-liability is recorded as a warrant liability in the condensed consolidated balance sheets and is subject to re-measurement to fair value at each balance sheet date, with any changes in fair value recognized in the condensed consolidated statements of operations and comprehensive loss. If the debt is retired early, the associated debt discount is then recognized immediately as interest expense in the condensed consolidated statements of operations and comprehensive loss.
Convertible Debt
In accordance with ASU 2020-06, Debt—Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic 815-40): Accounting for Convertible Instruments and Contracts in an Entity’s Own Equity, when we issue notes with conversion features, we evaluate if the conversion feature is freestanding or embedded. If the conversion feature is embedded, we do not separate the conversion feature from the host contract for convertible notes that are not required to be accounted for as derivatives, or that do not result in substantial premiums accounted for as paid-in-capital. Consequently, we account for a convertible note as a single liability measured at its amortized cost as long as no other features require separation and recognition as derivatives. If the conversion feature is freestanding, or is embedded and meets the requirements to be separated, we account for the conversion feature as a derivative under ASC 815, Derivatives and Hedging (“ASC 815”). We record the derivative instrument at fair value at inception, and subsequently re-measure to fair value at each reporting period and immediately prior to the extinguishment of the derivative instrument, with any changes recorded in the condensed consolidated statements of operations and comprehensive loss.
Leases
At inception of a contract, we determine if a contract meets the definition of a lease. We determine if the contract conveys the right to control the use of an identified asset for a period of time. We assess throughout the period of use whether we have both of the following: (i) the right to obtain substantially all the economic benefits from use of the identified asset, and (ii) the right to direct the use of the identified asset. This determination is reassessed if the terms of the contract are changed. Leases are classified as operating or finance leases based on the terms of the lease agreement and certain characteristics of the identified asset. Right-of-use assets and lease liabilities are recognized at the lease commencement date based on the present value of the future lease payments less any lease incentives received. At the lease commencement date, the discount rate implicit in the lease is used to discount the lease liability if readily determinable. If not readily determinable or leases do not contain an implicit rate, our incremental borrowing rate is used as the discount rate. Our policy is to not record leases with an original term of twelve months or less within the condensed consolidated balance sheets and we recognize lease expense for these short-term leases on a straight-line basis over the lease term.
Certain lease agreements may require us to pay additional amounts for taxes, insurance, maintenance, and other expenses, which are generally referred to as non-lease components. Such variable non-lease components are treated as variable lease payments and recognized in the period in which the obligation for these payments is incurred. Variable lease components and variable non-lease components are not measured as part of the right-of-use asset and liability. Only when lease components and their associated non-lease components are fixed are they accounted for as a single lease component and are recognized as part of a right-of-use asset and liability. Total contract consideration is allocated to the fixed lease and non-lease component. This policy election applies consistently to all asset classes under lease agreements.
Leases may contain clauses for renewal at our option. Payments to be made in option periods are recognized as part of the right-of-use lease assets and lease liabilities when it is reasonably certain that the option to extend the lease will be exercised, or is not at our option. We determine whether the reasonably certain threshold is met by considering contract-, asset-, market-, and entity-based factors. Operating lease expense, which is recognized on a straight-line basis over the lease term, and the amortization of finance lease right-of-use assets, which are included in property and equipment and depreciated, are included in research and development or general and administrative expenses consistent with the leased assets’ primary use. Accretion on the liabilities for finance leases is included in interest expense.
Contingent Earn-Out Liabilities
In connection with the Reverse Recapitalization, certain Clene Nanomedicine stockholders are entitled to receive additional shares of Common Stock (the “Clene Nanomedicine Contingent Earn-out”) as follows: (i)
In accordance with ASC 815, the Contingent Earn-outs are not indexed to our own stock and therefore were accounted for as a liability at the Reverse Recapitalization date and are subsequently remeasured to fair value at each reporting date with changes recorded as a component of other income (expense), net. As of June 30, 2025 and December 31, 2024, the Contingent Earn-outs had no value as determined using a Monte Carlo valuation model in order to simulate the future path of our stock price over the earn-out periods.
Common Stock Warrants
We account for common stock warrants as either equity- or liability-classified instruments based on an assessment of the warrant terms. The assessment considers whether the warrants are freestanding financial instruments pursuant to ASC 480, meet the definition of a liability pursuant to ASC 480, and whether the warrants meet all the requirements for equity classification under ASC 815, including whether the warrants are indexed to our Common Stock, among other conditions for equity classification. This assessment, which requires the use of professional judgment, is conducted at the time of warrant issuance and, for liability-classified warrants, at each reporting period end date while the warrants are outstanding.
Grant Funding
We may submit applications to receive grant funding from governmental and non-governmental entities. We account for grants by analogizing to the grant accounting model under IAS 20, Accounting for Government Grants and Disclosure of Government Assistance (“IAS 20”). We recognize grant funding without conditions or continuing performance obligations, including certain research and development tax credits, as other income in the condensed consolidated statements of operations and comprehensive loss. We accrue certain research and development tax credits receivable in other current assets (see Note 4) in an amount equal to the qualifying expenses incurred in each period multiplied by the applicable reimbursement percentage and we recognize other income in the condensed consolidated statements of operations and comprehensive loss. After submission of our tax returns, we receive a cash refund of certain research and development tax credits and relieve the receivable.
We recognize grant funding with conditions or continuing performance obligations as a reduction in research and development or general and administrative expenses in the period during which the related qualifying expenses are incurred and as the conditions or performance obligations are fulfilled. Any amount received in advance of fulfilling such conditions or performance obligations is recorded in accrued liabilities (see Note 6) if the conditions or performance obligations are expected to be met within the next twelve months. We recognized grant funding as a reduction of research and development expenses totaling $
In October 2023 we were awarded a grant (“the NIH Grant”) in collaboration with Columbia University, the prime awardee, and Synapticure, a neurology specialty health clinic, from the National Institutes of Health (“NIH”). The NIH Grant was awarded pursuant to the Accelerating Access to Critical Therapies for ALS Act to support up to a four-year Expanded Access Program (the “ACT-EAP”) for CNM-Au8® treatment of ALS. The NIH Grant totaled $
Foreign Currency Translation and Transactions
Our functional and reporting currency is the U.S. dollar (“USD”). Clene Australia and Clene Netherlands determined their functional currencies to be the Australian dollar and Euro, respectively. The results of our foreign currency operations are translated into USD at the average exchange rates during the period, assets and liabilities are translated using the exchange rate as of the balance sheet date, and stockholders’ deficit is translated using historical rates. Adjustments from the translation of the results of our foreign currency operations are excluded from net loss and are accumulated in a separate component of stockholders’ deficit. We also incur foreign exchange transaction gains and losses for purchases denominated in foreign currencies. Foreign exchange transaction gains and losses are included in other income (expense), net, as incurred.
Comprehensive Loss
Comprehensive loss includes net loss as well as other changes in stockholders’ deficit that result from transactions and economic events other than those with stockholders. The only elements of other comprehensive loss in any periods presented were the translation of foreign currency denominated balances of Clene Australia and Clene Netherlands to USD for consolidation and the unrealized loss on available-for-sale securities.
Net Loss Per Share Attributable to Common Stockholders
Basic net loss per share attributable to common stockholders is calculated using our weighted-average outstanding common shares. Shares issuable for little or no cash consideration, such as pre-funded warrants, shall be considered outstanding common shares upon the satisfaction of any contingent conditions or when there are no contingent conditions. Diluted net loss per share attributable to common stockholders is calculated using our weighted-average outstanding common shares including the dilutive effect of securities as determined under the treasury stock method, except for the dilutive effect of convertible notes payable, which is calculated under the if-converted method, even if the embedded conversion option is out-of-the-money. In periods in which we report a net loss attributable to common stockholders, diluted net loss per share attributable to common stockholders is the same as basic net loss per share attributable to common stockholders, since dilutive common shares are not assumed to have been issued if their effect is anti-dilutive.
Segment Information
We report segment information based on ASC 280 Segment Reporting (“ASC 280”), which defines operating segments as components of a company that engage in activities from which it may recognize revenues and incur expenses, and for which operating results are regularly reviewed by the entity’s chief operating decision maker (“CODM”) to make decisions regarding resource allocation and assess performance, and for which discrete financial information is available. We determined that the Company is a single operating and reportable segment (“Products”) focused on treating central nervous system disorders through discovery, development, and commercialization of our novel CSN therapeutics. Our chief executive officer acts as the CODM and allocates resources and assesses performance at a consolidated level. Segment information is further described in Note 16.
Income Taxes
We account for income taxes using the asset and liability method, which requires the recognition of deferred tax assets and liabilities for the expected future tax consequences of events that have been recognized in the condensed consolidated financial statements or in our tax returns. Deferred tax assets and liabilities are determined based on the differences between the financial statement basis and tax basis of assets and liabilities using enacted tax rates in effect for the year in which the differences are expected to reverse. Changes in deferred tax assets and liabilities are recorded in the provision for income taxes. We assess the likelihood that our deferred tax assets will be recovered from future taxable income and, to the extent we believe, based upon the weight of available evidence, that it is more likely than not that all or a portion of the deferred tax assets will not be realized, a valuation allowance is established through a charge to income tax expense. Potential for recovery of deferred tax assets is evaluated by estimating the future taxable profits expected and considering prudent and feasible tax planning strategies.
We account for uncertainty in income taxes recognized in the condensed consolidated financial statements by applying a two-step process to determine the amount of tax benefit to be recognized. First, the tax position must be evaluated to determine the likelihood that it will be sustained upon external examination by the taxing authorities. If the tax position is deemed more-likely-than-not to be sustained, the tax position is then assessed to determine the amount of benefit to recognize in the condensed consolidated financial statements. The amount of the benefit that may be recognized is the largest amount that has a greater than 50% likelihood of being realized upon ultimate settlement. The provision for income taxes includes the effects of any resulting tax reserves, or unrecognized tax benefits, which are considered appropriate as well as the related net interest and penalties.
Stock-Based Compensation
We account for stock-based compensation arrangements using a fair value-based method for costs related to all share-based payments including stock options and stock awards. Stock-based compensation expense is recorded in research and development and general and administrative expenses based on the classification of the work performed by the grantees. The fair value is recognized over the period during which a grantee is required to provide services in exchange for the option award and service-based stock awards, known as the requisite service period (usually the vesting period), on a straight-line basis. For stock awards with market conditions, the fair value is recognized over the period based on the expected milestone achievement dates as the derived service period (usually the vesting period), on a straight-line basis. For stock awards with performance conditions, the grant-date fair value of these awards is the market price on the applicable grant date, and compensation expense will be recognized when the conditions become probable of being satisfied. We recognize a cumulative true-up adjustment once the conditions become probable of being satisfied as the related service period had been completed in a prior period. We generally grant stock options with a four-year requisite service period. Certain stock options may vest based upon performance conditions instead of service conditions, such as the achievement of regulatory milestones or financial performance measures. For the grant-date fair value, we estimate the expected term of stock options with performance conditions based upon the nature of the conditions. If the expected term is not estimable and the achievement of performance conditions is not probable, we use the contractual term as the expected term. We elect to account for forfeitures as they occur, rather than estimating expected forfeitures. We determine the fair value of stock option awards using a Black-Scholes option pricing model based on the closing price of our Common Stock as reported by Nasdaq on the date of grant. The fair value of stock awards with market conditions are determined using a Monte Carlo valuation model.
Recent Accounting Pronouncements Not Yet Adopted
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures (“ASU 2023-09”). ASU 2023-09 requires, among other things, that public entities on an annual basis disclose specific categories of the tax rate reconciliation, provide additional information for reconciling items that meet a quantitative threshold, and disclose income taxes paid disaggregated by jurisdiction. The guidance is effective for annual periods beginning after December 15, 2024. We are currently evaluating the impact of ASU 2023-09.
In November 2024, the FASB issued ASU 2024-03, Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses (“ASU 2024-03”). ASU 2024-03 requires that public entities disclose additional information about specific expense categories in the notes to financial statements at interim and annual reporting periods. In January 2025, the FASB clarified the effective date of ASU 2024-03 with the issuance of ASU 2025-01, Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic 220-40): Clarifying the Effective Date (“ASU 2025-01”). The guidance is effective for annual periods beginning after December 15, 2026, and interim periods within annual periods beginning after December 15, 2027, with early adoption permitted. We are currently evaluating the impact of ASU 2024-03.
Note 3. Cash and Cash Equivalents
Cash and cash equivalents as of June 30, 2025 were as follows:
| June 30, 2025 | ||||||||||||||||
| (in thousands) | Amortized Cost | Gross Unrealized Gains | Gross Unrealized Losses | Fair Value | ||||||||||||
| Cash equivalents (contractual maturity within 90 days): | ||||||||||||||||
| Money market funds | $ | $ | $ | $ | ||||||||||||
| Total cash equivalents | ||||||||||||||||
| Cash | ||||||||||||||||
| Total cash and cash equivalents | $ | $ | $ | $ | ||||||||||||
Cash and cash equivalents as of December 31, 2024 were as follows:
| December 31, 2024 | ||||||||||||||||
| (in thousands) | Amortized Cost | Gross Unrealized Gains | Gross Unrealized Losses | Fair Value | ||||||||||||
| Cash equivalents (contractual maturity within 90 days): | ||||||||||||||||
| Money market funds | $ | $ | $ | $ | ||||||||||||
| Total cash equivalents | ||||||||||||||||
| Cash | ||||||||||||||||
| Total cash and cash equivalents | $ | $ | $ | $ | ||||||||||||
Note 4. Prepaid Expenses and Other Current Assets
Prepaid expenses and other current assets as of June 30, 2025 and December 31, 2024 were as follows:
| June 30, |
December 31, |
|||||||
| (in thousands) |
2025 |
2024 |
||||||
| Metals to be used in research and development |
$ | $ | ||||||
| Grants receivable |
||||||||
| Prepaid clinical and CRO expenses |
||||||||
| Research and development tax credits receivable |
||||||||
| Other |
||||||||
| Total prepaid expenses and other current assets |
$ | $ | ||||||
Note 5. Property and Equipment, Net
Property and equipment, net, as of June 30, 2025 and December 31, 2024 were as follows:
| June 30, |
December 31, |
|||||||
| (in thousands) |
2025 |
2024 |
||||||
| Lab equipment |
$ | $ | ||||||
| Office equipment |
||||||||
| Computer software |
||||||||
| Leasehold improvements |
||||||||
| Construction in progress |
||||||||
| Less accumulated depreciation |
( |
) | ( |
) | ||||
| Total property and equipment, net |
$ | $ | ||||||
Depreciation expense recorded in research and development expense and general and administrative expense during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| General and administrative |
$ | $ | $ | $ | ||||||||||||
| Research and development |
||||||||||||||||
| Total depreciation expense |
$ | $ | $ | $ | ||||||||||||
Note 6. Accrued Liabilities
Accrued liabilities as of June 30, 2025 and December 31, 2024 were as follows:
| June 30, |
December 31, |
|||||||
| (in thousands) |
2025 |
2024 |
||||||
| Accrued compensation and benefits |
$ | $ | ||||||
| Deferred grants |
||||||||
| Accrued CRO and clinical fees |
||||||||
| Other |
||||||||
| Total accrued liabilities |
$ | $ | ||||||
Note 7. Leases
We lease laboratory and office space and certain laboratory equipment under non-cancellable operating leases. The carrying value of our right-of-use lease assets is substantially concentrated in our real estate leases, while the volume of lease agreements is primarily concentrated in equipment leases. We expect that, in the normal course of business, the existing leases will be renewed or replaced by similar leases.
We have leases for
As of June 30, 2025 and December 31, 2024, our operating lease obligations had a weighted-average discount rate of
Maturity Analysis of Lease Obligations
The maturity analysis of our operating lease obligations as of June 30, 2025 was as follows:
| (in thousands) |
Operating Leases |
|||
| 2025 (remainder) |
$ | |||
| 2026 |
||||
| 2027 |
||||
| 2028 |
||||
| 2029 |
||||
| 2030 |
||||
| Thereafter |
||||
| Total minimum lease payments |
||||
| Less amount representing interest/discounting |
( |
) | ||
| Present value of minimum lease payments |
||||
| Less lease obligations, current portion |
( |
) | ||
| Lease obligations, net of current portion |
$ | |||
Components of Lease Cost
The components of lease costs for the three and six months ended June 30, 2025 and 2024 were as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| Finance lease amortization |
$ | $ | $ | $ | ||||||||||||
| Operating lease costs |
||||||||||||||||
| Short-term lease costs |
||||||||||||||||
| Variable lease costs |
||||||||||||||||
| Total lease costs |
$ | $ | $ | $ | ||||||||||||
Supplemental Cash Flow Information
| Six Months Ended June 30, | ||||||||
| (in thousands) | 2025 | 2024 | ||||||
| Operating cash flows from operating leases | $ | ( | ) | $ | ( | ) | ||
| Financing cash flows from finance leases | $ | $ | ( | ) | ||||
Note 8. Notes Payable and Convertible Notes Payable
Our notes payable and convertible notes payable as of June 30, 2025 and December 31, 2024 was as follows:
| Stated | June 30, | December 31, | ||||||||||
| (in thousands, except interest rates) | Interest Rate | 2025 | 2024 | |||||||||
| Notes payable: | ||||||||||||
| Advance Cecil, Inc. (commenced April 2019) | % | $ | $ | |||||||||
| Maryland DHCD (commenced February 2019) | % | |||||||||||
| Maryland DHCD (commenced May 2022) | % | |||||||||||
| Senior Secured Promissory Notes (commenced December 2024) | % | |||||||||||
| Unamortized discount and debt issuance costs | ( | ) | ( | ) | ||||||||
| Less notes payable, current portion, net of unamortized discount and debt issuance costs | ( | ) | ( | ) | ||||||||
| Notes payable, net of current portion | $ | $ | ||||||||||
| Convertible notes payable: | ||||||||||||
| Maryland DHCD (commenced December 2022) | % | $ | $ | |||||||||
| Senior Secured Convertible Promissory Notes (commenced December 2024) | % | |||||||||||
| Unamortized discount and debt issuance costs | ( | ) | ( | ) | ||||||||
| Convertible notes payable | $ | $ | ||||||||||
Maryland Loans
In April 2019, we entered into a term loan agreement (the “2019 Cecil Loan”) with Advance Cecil Inc., a non-stock corporation formed under the laws of the State of Maryland, for $
In February 2019, we entered into a term loan agreement (the “2019 MD Loan”) with the Department of Housing and Community Development (“DHCD”), a principal department of the State of Maryland, for $
In May 2022, we entered into a term loan agreement (the “2022 MD Loan”) with DHCD for up to $
In December 2022, we entered into a term loan agreement (the “2022 DHCD Loan”) with DHCD for $
Avenue Loan
In May 2021, we entered into a term loan agreement (the “2021 Avenue Loan”) with Avenue Venture Opportunities Fund, L.P. (“Avenue”) for up to $
On September 30, 2024, we entered into an amendment (the “Third Amendment”) that (i) reduced the October 2024 principal installment from $
We recognized interest expense of $
At the inception of the 2021 Avenue Loan, we issued a warrant to Avenue to purchase Common Stock (the “2021 Avenue Warrant”). A portion of the net proceeds at issuance of the 2021 Avenue Loan were allocated to the 2021 Avenue Warrant in an amount equal to its fair value of $
Senior Secured Convertible Promissory Notes
In December 2024, we entered into a note purchase agreement (the “Note Purchase Agreement”) pursuant to which we sold the 2024 SSCP Notes in a principal amount totaling $
We are subject to covenants until maturity, including a requirement to maintain unrestricted cash and cash equivalents of at least $
The Holders may, in their sole discretion, convert up to
We are required to file and maintain an effective registration statement covering the resale of the shares underlying the SSCPN Conversion Feature or we shall pay the Holders a penalty equal to
Debt Maturities
Future debt payments, net of unamortized discounts and debt issuance costs, without giving effect to any potential future exercise of equity conversion features, and without giving effect to an amendment to the 2024 SSCP Notes which occurred subsequent to June 30, 2025 (see Note 17), are as follows:
| (in thousands) | 2019 MD Loan | 2019 Cecil Loan | 2022 MD Loan | 2022 DHCD Loan | 2024 SSCP Notes | Total | ||||||||||||||||||
| 2025 (remainder) | $ | $ | $ | $ | $ | |||||||||||||||||||
| 2026 | ||||||||||||||||||||||||
| 2027 | ||||||||||||||||||||||||
| 2028 | ||||||||||||||||||||||||
| 2029 | ||||||||||||||||||||||||
| 2030 | ||||||||||||||||||||||||
| Thereafter | ||||||||||||||||||||||||
| Total debt principal payments | ||||||||||||||||||||||||
| Accrued and unpaid interest | ||||||||||||||||||||||||
| Unamortized discount and debt issuance costs | ( | ) | ( | ) | ( | ) | ( | ) | ||||||||||||||||
| Future debt payments, net | $ | $ | $ | $ | $ | $ | ||||||||||||||||||
Note 9. Commitments and Contingencies
Commitments
We enter into agreements in the normal course of business with CROs for clinical trials and with vendors for preclinical studies and other services and products for operating purposes, which are cancelable at any time by us, subject to payment of our remaining obligations under binding purchase orders and, in certain cases, nominal early termination fees. These commitments are not deemed significant.
As of June 30, 2025 and December 31, 2024, we had commitments under various agreements for capital expenditures totaling $
Contingencies
From time to time, we may have certain contingent legal liabilities that arise in the ordinary course of business activities. We accrue a liability for such matters when it is probable that future expenditures will be made, and such expenditures can be reasonably estimated. We are not aware of any current material pending legal matters or claims.
We received two grants from the National Multiple Sclerosis Society (“NMSS”): (i) $
We account for the SSCPN Collateral Deficiency Fee and SSCPN Registration Fee (see Note 8) as contingent liabilities that were not probable as of June 30, 2025, and therefore no contingent liabilities were recorded. Our estimate of the possible range of loss for the SSCPN Registration Fee is between $
Note 10. Income Taxes
The components of loss before income taxes for the three and six months ended June 30, 2025 and 2024 were as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| United States |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Foreign |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Net loss before income taxes |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
We are subject to taxation in the U.S., Australia, Netherlands, and various state jurisdictions. Our tax returns from 2018 to present are subject to examination by the U.S. and state authorities due to the carry forward of unutilized net operating losses and research and development credits. There are currently no pending examinations. We compute our quarterly income tax provision by using a forecasted annual effective tax rate and adjust for any discrete items arising during the quarter. The primary difference between the effective tax rate and the federal statutory tax rate relates to the full valuation allowance on our net operating losses and other deferred tax assets.
Note 11. Benefit Plans
401(k) Plan
Our 401(k) plan is a deferred salary arrangement under Section 401(k) of the Internal Revenue Code. We match
Stock Compensation Plans
The Clene Nanomedicine, Inc. 2014 Stock Plan (the “2014 Plan”) was adopted in July 2014. Effective as of the closing of the Reverse Recapitalization, no additional awards may be granted under the 2014 Plan. As of June 30, 2025, a total of
The Clene Inc. 2020 Amended Stock Plan (the “2020 Plan”) was adopted in December 2020 and amended in May 2023, May 2024, and May 2025. Currently,
Stock-Based Compensation Expense
Stock-based compensation expense recorded in research and development expense and general and administrative expense during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| (in thousands) | 2025 | 2024 | 2025 | 2024 | ||||||||||||
| General and administrative | $ | $ | $ | $ | ||||||||||||
| Research and development | ||||||||||||||||
| Total stock-based compensation expense | $ | $ | $ | $ | ||||||||||||
Stock-based compensation expense by award type during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| (in thousands) | 2025 | 2024 | 2025 | 2024 | ||||||||||||
| Stock options | $ | $ | $ | $ | ||||||||||||
| Stock awards | ( | ) | ( | ) | ||||||||||||
| Total stock-based compensation expense | $ | $ | $ | $ | ||||||||||||
Stock Options
Outstanding stock options and related activity during the six months ended June 30, 2025 was as follows:
| (in thousands, except share, per share, and term data) | Number of Options | Weighted Average Exercise Price Per Share | Weighted Average Remaining Term (Years) | Intrinsic Value | ||||||||||||
| Outstanding – December 31, 2024 | $ | $ | ||||||||||||||
| Granted | — | |||||||||||||||
| Forfeited | ( | ) | — | — | ||||||||||||
| Expired | ( | ) | — | — | ||||||||||||
| Outstanding – June 30, 2025 | $ | $ | ||||||||||||||
| Vested and exercisable – June 30, 2025 | $ | $ | ||||||||||||||
| Vested, exercisable or expected to vest – June 30, 2025 | $ | $ | ||||||||||||||
As of June 30, 2025 and December 31, 2024, we had approximately $
The weighted-average grant-date fair value of stock options granted during the six months ended June 30, 2025 and 2024 was $
| Six Months Ended June 30, | ||||||||
| 2025 | 2024 | |||||||
| Expected stock price volatility | % | % | ||||||
| Risk-free interest rate | % | % | ||||||
| Expected dividend yield | % | % | ||||||
| Expected term of options (in years) | ||||||||
Stock Awards
Stock awards include rights to restricted stock awards with market-based vesting conditions and restricted stock units with service-based vesting conditions. We had no activity related to outstanding stock awards during the six months ended June 30, 2025. Outstanding stock awards and related activity during the six months ended June 30, 2025 was as follows:
| Number of Stock Awards | Weighted Average Grant Date Fair Value | |||||||
| Unvested balance – December 31, 2024 | $ | |||||||
| Forfeited | ( | ) | ||||||
| Unvested balance – June 30, 2025 | $ | |||||||
As of June 30, 2025 and December 31, 2024, we had unrecognized stock-based compensation cost related to unvested stock awards.
Note 12. Fair Value
Cash and cash equivalents are carried at fair value. Financial instruments, including accounts receivable, accounts payable, and accrued expenses are carried at cost, which approximates fair value given their short-term nature. Our remaining fair value measures are discussed below.
Financial Instruments with Fair Value Measurements on a Recurring Basis
The fair value hierarchy for financial instruments measured at fair value on a recurring basis as of June 30, 2025 was as follows:
| June 30, 2025 |
||||||||||||||||
| (in thousands) |
Level 1 |
Level 2 |
Level 3 |
Total |
||||||||||||
| Cash equivalents: |
||||||||||||||||
| Money market funds |
$ | $ | $ | $ | ||||||||||||
| Common stock warrant liabilities |
||||||||||||||||
| Derivative liabilities |
||||||||||||||||
The fair value hierarchy for financial instruments measured at fair value on a recurring basis as of December 31, 2024 was as follows:
| December 31, 2024 |
||||||||||||||||
| (in thousands) |
Level 1 |
Level 2 |
Level 3 |
Total |
||||||||||||
| Cash equivalents: |
||||||||||||||||
| Money market funds |
$ | $ | $ | $ | ||||||||||||
| Common stock warrant liabilities |
||||||||||||||||
| Derivative liabilities |
||||||||||||||||
There were no transfers between Level 1, Level 2, or Level 3 during any of the periods above.
Changes in the fair value of our Level 3 financial instruments during the six months ended June 30, 2025 were as follows:
| (in thousands) |
Common Stock Warrant Liabilities |
Derivative Liabilities |
||||||
| Balance – December 31, 2024 |
$ | $ | ||||||
| Change in fair value |
( |
) | ( |
) | ||||
| Balance – June 30, 2025 |
$ | $ | ||||||
Changes in the fair value of our Level 3 financial instruments during the six months ended June 30, 2024 were as follows:
| (in thousands) |
Common Stock Warrant Liabilities |
Clene Nanomedicine Contingent Earn-out |
Initial Stockholders Contingent Earn-out |
|||||||||
| Balance – December 31, 2023 |
$ | $ | $ | |||||||||
| Change in fair value |
( |
) | ( |
) | ( |
) | ||||||
| Balance – June 30, 2024 |
$ | $ | $ | |||||||||
Valuation of Notes Payable and Convertible Notes Payable
Our notes payable and convertible notes payable are categorized within Level 3 of the fair value hierarchy. The 2019 MD Loan and 2019 Cecil Loan are carried at the greater of principal plus accrued interest or the value of the Phantom Shares (see Note 8), which approximates fair value. The 2022 MD Loan and 2022 DHCD Loan are carried at amortized cost, which approximates fair value due to our credit risk and market interest rates.
The 2024 SSCP Notes are carried at their amortized cost of $
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
% | % | ||||||
| Risk-free interest rate |
% | % | ||||||
| Expected dividend yield |
% | % | ||||||
| Expected term (in years) |
||||||||
| Probability of change of control |
% | % | ||||||
| Probability of dissolution |
% | % | ||||||
| Probability of other outcome |
% | % | ||||||
Valuation of the Common Stock Warrant Liabilities
The 2023 Avenue Warrant, as amended, is classified as a liability and carried at fair value. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) settlement of the instrument upon a change of control transaction, (ii) dissolution of the Company, or (iii) another outcome outside of (i)-(ii). These estimates require significant judgment. The carrying amount may fluctuate significantly and the actual settlement amount may be materially different from the estimated fair value. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
% | % | ||||||
| Risk-free interest rate |
% | % | ||||||
| Expected dividend yield |
% | % | ||||||
| Expected term (in years) |
||||||||
| Probability of change of control |
% | % | ||||||
| Probability of dissolution |
% | % | ||||||
| Probability of other outcome |
% | % | ||||||
The Tranche A Warrants are classified as a liability and carried at fair value. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) acceptance of a new drug application (“NDA”) by the U.S. Food and Drug Administration (“FDA”) for CNM-Au8, (ii) settlement upon a fundamental transaction, (iii) dissolution of the Company, and (iv) another outcome outside of (i)-(iii). These estimates require significant judgment. The carrying amount may fluctuate significantly and the actual settlement amount may be materially different from the estimated fair value. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
% | % | ||||||
| Risk-free interest rate |
% | % | ||||||
| Expected dividend yield |
% | % | ||||||
| Expected term (in years) |
||||||||
| Probability of NDA acceptance |
% | % | ||||||
| Probability of fundamental transaction |
% | % | ||||||
| Probability of dissolution |
% | % | ||||||
| Probability of other outcome |
% | % | ||||||
The 2024 Common Warrants are classified as a liability and carried at fair value. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) dissolution of the Company and (ii) another outcome outside of dissolution. These estimates require significant judgment. The carrying amount may fluctuate significantly and the actual settlement amount may be materially different from the estimated fair value. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
% | % | ||||||
| Risk-free interest rate |
% | % | ||||||
| Expected dividend yield |
% | % | ||||||
| Expected term (in years) |
||||||||
| Probability of dissolution |
% | % | ||||||
| Probability of other outcome |
% | % | ||||||
Note 13. Capital Stock
As of June 30, 2025 and December 31, 2024, our amended and restated certificate of incorporation authorized us to issue
Our common stockholders are entitled to one vote per share and to notice of any stockholders’ meeting. Voting, dividend, and liquidation rights of the holders of Common Stock are subject to the prior rights of holders of all classes of stock and are qualified by the rights, powers, preferences, and privileges of the holders of Preferred Stock. No distributions shall be made with respect to Common Stock until all declared dividends to Preferred Stock have been paid or set aside for payment. Common Stock is not redeemable at the option of the holder.
Common Stock Warrants
We have issued the following outstanding warrants and pre-funded warrants to purchase shares of Common Stock:
| Number of Shares Issuable | |||||||||||||||||
| June 30, | December 31, | ||||||||||||||||
| Date Exercisable | Exercise Price | Expiration | Classification | 2025 | 2024 | ||||||||||||
| December 2020 | $ | December 2025 | (1 | ) | Equity | ||||||||||||
| December 2020 | $ | December 2025 | (2 | ) | Equity | ||||||||||||
| June 2023 | $ | June 2028 | (3 | ) | Liability | ||||||||||||
| June 2023 | $ | June 2026 | (4 | ) | Liability | ||||||||||||
| June 2023 | $ | June 2030 | (5 | ) | Equity | ||||||||||||
| October 2024 | $ | None | (6 | ) | Equity | ||||||||||||
| October 2024 | $ | October 2029 | (7 | ) | Liability | ||||||||||||
| Total shares | |||||||||||||||||
| (1) | Represents |
| (2) | Represents |
| (3) | Represents |
| (4) | Represents |
| (5) | Represents |
| (6) | Represents |
| (7) | Represents |
Public Offerings
In October 2024, pursuant to a placement agency agreement with Canaccord Genuity LLC (“Canaccord”), we sold
Common Stock Sales Agreement
In April 2022, we entered into an equity distribution agreement (the “2022 ATM Agreement”), which we amended in December 2022. In April 2025, we entered into an equity distribution agreement (the “2025 ATM Agreement,” and collectively with the 2022 ATM Agreement, the “ATM Agreements”). Canaccord acts as placement agent under the ATM Agreements and we may offer and sell shares of Common Stock from time to time through Canaccord. The issuance and sale of Common Stock by us under the 2022 ATM Agreement was made pursuant to our registration statement on Form S-3 (file number 333-264299), declared effective by the SEC on April 26, 2022, and a related prospectus supplement, which expired on April 26, 2025. The issuance and sale of Common Stock by us under the 2025 ATM Agreement was made pursuant to our registration statement on Form S-3 (file number 333-286058), declared effective by the SEC on April 25, 2025, and a related prospectus supplement.
Pursuant to the ATM Agreements, Canaccord is not required to sell any specific number or dollar amount of Common Stock but will act as our placement agent to sell, on our behalf, all of the Common Stock requested by us to be sold, consistent with Canaccord’s normal trading and sales practices, on terms mutually agreed between Canaccord and us, for a fixed commission from each sale of Common Stock, if any. During the three and six months ended June 30, 2025, we sold
Common Stock Purchase Agreement
On March 3, 2023, we entered into a purchase agreement (the “Purchase Agreement”) with Lincoln Park Capital Fund, LLC (“Lincoln Park”), pursuant to which Lincoln Park committed to purchase up to $
On the date of the Purchase Agreement, we issued
We evaluated the Purchase Agreement under ASC 815-40 Derivatives and Hedging—Contracts on an Entity's Own Equity as it represents the right to require Lincoln Park to purchase shares of Common Stock in the future, similar to a put option. We concluded it represents a freestanding derivative instrument that does not qualify for equity classification and therefore requires fair value accounting. We analyzed the terms of the contract and concluded the derivative instrument has value as of June 30, 2025 and December 31, 2024. We did not effect any sales during the periods presented herein.
Note 14. Net Loss Per Share
The computation of basic and diluted net loss per share attributable to common stockholders for the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands, except share and per share data) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| Numerator: |
||||||||||||||||
| Net loss attributable to common stockholders |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Denominator: |
||||||||||||||||
| Weighted average common shares outstanding |
||||||||||||||||
| Net loss per share attributable to common stockholders – basic and diluted |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
The following shares of potentially dilutive securities were excluded from the computation of diluted net loss per share attributable to common stockholders for the three and six months ended June 30, 2025 and 2024 because they were antidilutive, out-of-the-money, or the issuance of such shares is contingent upon certain conditions which were not satisfied by the end of the period:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| 2025 |
2024 |
2025 |
2024 |
|||||||||||||
| Convertible notes payable (see Note 8) |
||||||||||||||||
| Common stock warrants (see Note 13) |
||||||||||||||||
| Options to purchase common stock (see Note 11) |
||||||||||||||||
| Unvested restricted stock awards (see Note 11) |
||||||||||||||||
| Contingent earn-out shares (see Note 2) |
||||||||||||||||
| Total shares excluded from diluted net loss per share |
||||||||||||||||
Note 15. Related Party Transactions
Supply and License Agreements
In August 2018, we entered into an exclusive supply agreement (the “Supply Agreement”) and license agreement (the “License Agreement”) in conjunction with 4Life’s investment in the Series C preferred stock and warrants of our predecessor. On April 25, 2024, we entered into an amendment to the Supply Agreement and License Agreement (the “Amended 4Life Agreements”). The Amended 4Life Agreements contain the following terms:
| ● |
Supply Agreement. We granted 4Life, or its affiliates and mutually-agreed upon manufacturing vendors (the “Buyer Purchasing Parties”) an exclusive right to purchase certain of our dietary supplement and non-pharmaceutical products (the “Licensed Products”), and we shall exclusively sell the Licensed Products to the Buyer Purchasing Parties. The purchase price of Licensed Products shall be equal to our cost plus |
| ● |
License Agreement. We granted 4Life an exclusive, royalty bearing license to use, sell, and commercialize the Licensed Products. On a quarterly basis, 4Life shall pay us a royalty rate of |
We currently provide, on a non-exclusive basis, an aqueous zinc-silver ion dietary (mineral) supplement to 4Life, which is sold under the trade name Zinc Factor™, and an aqueous gold dietary (mineral) supplement of very low-concentration gold nanoparticles, that is sold by 4Life, on an exclusive basis, under the trade name Gold Factor™ and is subject to royalties. Total revenue under the Supply and License Agreements during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| Product revenue from related parties |
$ | $ | $ | $ | ||||||||||||
| Royalty revenue from related parties |
||||||||||||||||
| Total revenue from related parties |
$ | $ | $ | $ | ||||||||||||
Note 16. Geographic and Segment Information
Geographic Information
All of our long-lived assets, composed of property and equipment, net by location, were held in the U.S. as of June 30, 2025 and December 31, 2024. All of our revenues from external customers were generated in the U.S. during the three and six months ended June 30, 2025 and 2024.
Segment Information
Our Products segment measures of profit and loss is consolidated loss from operations, and its measure of total assets is consolidated total assets. Our CODM uses loss from operations predominantly in the annual budget and forecasting process to monitor variances in budget versus actual results along with consolidated total assets to determine resource allocation. Segment revenues from external customers, significant segment non-cash items, and other significant segment expense categories included within the measure of profit and loss and provided to our CODM were all based on their consolidated amounts. During the three and six months ended June 30, 2025 and 2024, these items were as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| Segment revenue from external customers |
$ | $ | $ | $ | ||||||||||||
| Segment operating expenses: |
||||||||||||||||
| Cost of revenue |
||||||||||||||||
| Research and development: |
||||||||||||||||
| CNM-Au8: |
||||||||||||||||
| Amyotrophic lateral sclerosis |
||||||||||||||||
| Multiple sclerosis |
||||||||||||||||
| Parkinsonʼs disease |
||||||||||||||||
| Regulatory activities |
||||||||||||||||
| General/pre-clinical/non-clinical |
||||||||||||||||
| CNM-ZnAg |
||||||||||||||||
| Facilities |
||||||||||||||||
| Depreciation |
||||||||||||||||
| Manufacturing |
||||||||||||||||
| Research |
||||||||||||||||
| Equipment |
||||||||||||||||
| Maintenance |
||||||||||||||||
| Information technology |
||||||||||||||||
| Personnel |
||||||||||||||||
| Stock-based compensation |
||||||||||||||||
| Grant revenue as a reduction of research and development expense |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Other segment items ‒ Research and development(1) |
||||||||||||||||
| General and administrative: |
||||||||||||||||
| Insurance |
||||||||||||||||
| Legal |
||||||||||||||||
| Finance and accounting |
||||||||||||||||
| Public and investor relations |
||||||||||||||||
| Facilities |
||||||||||||||||
| Depreciation |
||||||||||||||||
| Information technology |
||||||||||||||||
| Personnel |
||||||||||||||||
| Stock-based compensation |
||||||||||||||||
| Grant revenue as a reduction of general and administrative expense |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Other segment items ‒ General and administrative(2) |
||||||||||||||||
| Segment loss from operations |
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
| Reconciliation of segment loss from operations: |
||||||||||||||||
| Adjustments and reconciling items |
||||||||||||||||
| Consolidated loss from operations |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| (1) |
Includes expenses for travel, meals, dues, subscriptions, continuing education, and other miscellaneous expenses. |
| (2) | Includes expenses for travel, meals, dues, subscriptions, continuing education, lobbying, banking fees, postage, and other office and miscellaneous expenses. |
Our revenues during the three and six months ended June 30, 2025 and 2024 were predominantly with a single customer, 4Life, through our License and Supply Agreements (see Note 15). A reconciliation of the total of the Products segment loss from operations to consolidated net loss before income taxes for the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| (in thousands) |
2025 |
2024 |
2025 |
2024 |
||||||||||||
| Segment loss from operations |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| Total other income (expense), net(1) |
( |
) | ( |
) | ||||||||||||
| Net loss before income taxes |
$ | ( |
) | $ | ( |
) | $ | ( |
) | $ | ( |
) | ||||
| (1) |
Represents consolidated total other income (expense), net, as reported on the consolidated statements of operations and comprehensive loss. |
Products segment assets exclude corporate assets, such as cash, restricted cash, and corporate facilities. Total assets as of June 30, 2025 and December 31, 2024 were as follows:
| June 30, |
December 31, |
|||||||
| (in thousands) |
2025 |
2024 |
||||||
| Total assets: |
||||||||
| Products |
$ | $ | ||||||
| Corporate |
||||||||
| Consolidated |
$ | $ | ||||||
Additions to long-lived assets during the three and six months ended June 30, 2025 and 2024 were as follows:
| Six Months Ended June 30, |
||||||||
| (in thousands) |
2025 |
2024 |
||||||
| Products |
$ | $ | ||||||
| Corporate |
||||||||
| Consolidated |
$ | $ | ||||||
Note 17. Subsequent Events
Common Stock Sales Agreement
Subsequent to June 30, 2025, we sold
Amendment to December 2024 Senior Secured Convertible Promissory Notes
On August 13, 2025, we entered into an amendment to the 2024 SSCP Notes (the “Amended 2024 SSCP Notes”) with the Holders. Pursuant to the Amended 2024 SSCP Notes, the maturity date was extended to the earlier of (i) February 13, 2027 or (ii) upon a change in control transaction. The monthly repayments of $
August 2025 Senior Secured Convertible Promissory Notes
On August 13, 2025, we entered into a note purchase agreement (the “2025 Note Purchase Agreement”) pursuant to which we sold senior secured convertible promissory notes (the “2025 SSCP Notes”) in a principal amount totaling $
The holders of 2025 SSCP Notes may, in their sole discretion, convert up to
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
The following discussion and analysis of our financial condition and results of operations should be read in conjunction with our condensed consolidated financial statements and related notes included elsewhere in this Quarterly Report on Form 10-Q. This discussion contains forward-looking statements reflecting our or our management team’s expectations, hopes, beliefs, intentions, strategies, estimates, and assumptions concerning events and financial trends that may affect our future financial condition or results of operations. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. The words “anticipate,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “will,” “would,” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. Actual results and the timing of events may differ materially from those contained in these forward-looking statements due to a number of factors, including those discussed in the section titled “Risk Factors” in our Annual Report on Form 10-K. We undertake no obligation to update forward-looking statements to reflect events or circumstances after the date they were made, whether as a result of new information, future events, or otherwise, except as may be required under applicable securities laws. Unless the context otherwise requires, for purposes of this section, the terms the “Company,” “we,” “us,” or “our” are intended to mean the business and operations of Clene Inc. and its consolidated subsidiaries.
Business Overview
We are a clinical-stage pharmaceutical company pioneering the discovery, development, and commercialization of novel clean-surfaced nanotechnology (“CSN®”) therapeutics. CSN® therapeutics are comprised of atoms of transition elements that, when assembled in nanocrystal form, possess unusually high, unique catalytic activities not present in those same elements in bulk form. These catalytic activities drive, support, and maintain beneficial metabolic and energetic cellular reactions within diseased, stressed, and damaged cells.
Our patent-protected, proprietary position affords us the potential to develop a broad and deep pipeline of novel CSN therapeutics to address a range of diseases with high impact on human health. We innovated an electro-crystal-chemistry drug development platform that draws from advances in nanotechnology, plasma and quantum physics, material science, and biochemistry. Our platform process results in nanocrystals with faceted structures and surfaces that are free of the chemical surface modifications that accompany other production methods. Many traditional methods of nanoparticle synthesis involve the unavoidable deposition of potentially toxic organic residues and stabilizing surfactants on the particle surfaces. Synthesizing stable nanocrystals that are both nontoxic and highly catalytic has overcome this significant hurdle in harnessing transition metal catalytic activity for therapeutic use. Our clean-surfaced nanocrystals exhibit catalytic activities many-fold higher than other commercially available nanoparticles, produced using various techniques, that we have comparatively evaluated.
Our development and clinical efforts are dedicated to revolutionizing the treatment of neurodegenerative diseases to restore and protect neuronal health and function. Our nanotherapeutics target cellular energy impairments that are common to many diseases and we are currently focused on addressing the high unmet medical needs in central nervous system disorders including amyotrophic lateral sclerosis (“ALS”), multiple sclerosis (“MS”), and Parkinson’s disease (“PD”). We currently have no drugs approved for commercial sale and have not generated any revenue from drug sales. We have never been profitable and have incurred operating losses in each year since inception. We generate revenue from sales of dietary supplements through our wholly owned subsidiary, dOrbital, Inc., or through an exclusive license with 4Life Research LLC (“4Life”), an international supplier of health supplements, stockholder, and related party. We anticipate these revenues to be small compared to our operating expenses and to the revenue we expect to generate from potential future sales of our drug candidates, for which we are currently conducting clinical trials.
Reverse Recapitalization
Clene Nanomedicine, Inc. (“Clene Nanomedicine”) became a public company on December 30, 2020 (the “Closing Date”) when it completed a reverse recapitalization (the “Reverse Recapitalization”) with Tottenham Acquisition I Limited (“Tottenham”), and with Tottenham’s wholly-owned subsidiary and our predecessor, Chelsea Worldwide Inc., and Creative Worldwide Inc., a wholly-owned subsidiary of Chelsea Worldwide Inc. On the Closing Date, Chelsea Worldwide Inc. changed its name to Clene Inc. and listed its shares of common stock, par value $0.0001 per share (“Common Stock”) on the Nasdaq Capital Market (“Nasdaq”) under the symbol “CLNN.”
In connection with the Reverse Recapitalization, certain of Clene Nanomedicine’s common stockholders are entitled to receive earn-out payments (the “Clene Nanomedicine Contingent Earn-out”), and Tottenham’s former officers and directors and Norwich Investment Limited (collectively, the “Initial Stockholders”) are entitled to receive earn-out payments (the “Initial Stockholders Contingent Earn-out,” and both collectively the “Contingent Earn-outs”) based on achieving certain milestones.
Reverse Stock Split
Effective July 11, 2024 (the “Effective Date”), we filed a Certificate of Amendment to our Fourth Amended and Restated Certificate of Incorporation with the Secretary of State of the State of Delaware, to effect a 1-for-20 reverse stock split (the “Reverse Stock Split”) of our Common Stock. Beginning with the opening of trading on the Effective Date, our Common Stock began trading on Nasdaq on a split-adjusted basis under the same symbol, “CLNN.” As a result of the Reverse Stock Split, every 20 shares of our Common Stock issued and outstanding were automatically combined and converted into 1 validly issued, fully paid and non-assessable share of Common Stock. In lieu of any fractional shares, stockholders received an amount in cash (without interest) equal to: (i) the number of shares of Common Stock held by such stockholder before the Reverse Stock Split that would otherwise have been exchanged for such fractional shares multiplied by (ii) the closing price of our Common Stock on Nasdaq on the trading day immediately preceding the Effective Date.
The Reverse Stock Split did not reduce the total number of authorized shares of Common Stock or preferred stock, par value $0.0001 per share (“Preferred Stock”), or change the par values of the Company’s Common Stock or Preferred Stock. All outstanding stock options, warrants, rights to restricted stock awards, convertible debt, and contingent earn-out shares entitling their holders to purchase or receive shares of Common Stock were adjusted as a result of the Reverse Stock Split, in accordance with the terms of each such security. In addition, the number of shares reserved for issuance pursuant to our Amended 2020 Stock Plan was also appropriately adjusted. All historical share and per share data for the periods presented in our condensed consolidated financial statements, including for periods ending prior to July 11, 2024, has been adjusted to reflect the 1-for-20 Reverse Stock Split on a retroactive basis as if the Reverse Stock Split occurred as of the earliest period presented.
Recent Developments of Our Clinical Programs
Amyotrophic Lateral Sclerosis
In December 2024, we announced that we received written guidance from the Division of Neurology 1 (“DN1”) of the U.S. Food and Drug Administration (“FDA”) regarding a potential accelerated approval pathway for CNM-Au8® in ALS. As announced previously in September 2024, we were initially advised that the data presented in our briefing package for CNM-Au8 was not adequate to support an NDA submission under the accelerated approval pathway. However, following our November 2024 meeting with DN1 and presentation of additional data and analyses, the FDA provided guidance on a potential path to meet the regulatory standard for substantial evidence of effectiveness supporting accelerated approval. The FDA recommended that we investigate whether additional data from our ongoing compassionate use Expanded Access Programs (“EAPs”) could be leveraged to substantiate the effect of CNM-Au8 on neurofilament light (“NfL”) decline. We intend to follow the FDA’s recommendation to provide data from the ongoing EAPs and believe we can address the FDA’s requests. The additional NfL biomarker collection and analyses to support NDA submission is planned to be completed in the fourth quarter of 2025, as summarized below:
| ● |
NfL biomarker analyses—Provide supportive evidence of NfL declines in participants from our ongoing NIH-sponsored compassionate-use EAPs. We met with the FDA in the second quarter of 2025 to review our statistical analysis plan for the EAP NfL biomarker analyses, during which the FDA provided constructive feedback on our proposed analyses methodology. NfL change will be analyzed following nine months of treatment (primary NfL analysis) and after six months of treatment (supportive NfL analysis). These analyses are planned to provide supportive data of the NfL change demonstrated in the HEALEY ALS Platform Trial double-blind period following six months of treatment with CNM-Au8. |
| ● |
Survival pharmacometric modeling—Provide analyses of NfL and related disease-specific biomarkers linked to clinical survival benefit and clinical changes from the Phase 2 trial data. |
| ● |
Additional ALS-specific biomarkers—Provide analyses of additional ALS-disease specific biomarkers to support the pharmacodynamic activity of CNM-Au8 for treatment of ALS. |
The FDA noted that whether NfL can serve as a reasonably likely surrogate endpoint for the effects of CNM-Au8 in ALS and whether the magnitude of change observed on NfL in patients treated with CNM-Au8 is reasonably likely to predict clinical benefit for ALS would be a matter of review. The FDA has confirmed an additional Type C meeting with us to occur in the third quarter of 2025 to review the long-term survival benefit from CNM-Au8 30 mg treatment compared to concurrently randomized controls from another HEALEY ALS Platform Trial Regimen, assessing whether these data support filing of an NDA under an accelerated approval pathway. Assuming the NfL data from our ongoing EAP funded by a National Institutes of Health grant (the “ACT-EAP”) is concordant with NfL results shown in the HEALEY ALS Platform Trial, we plan to submit an NDA by the end of 2025 under an accelerated approval pathway. We also plan to commence a confirmatory Phase 3 trial, RESTORE-ALS, in the first half of 2026, contingent on funding. The trial is designed to investigate the effects of CNM-Au8 on improved survival (primary endpoint) and delayed time to ALS clinical worsening events (secondary efficacy endpoint).
Multiple Sclerosis
We have initiated a second dosing cohort of REPAIR-MS, an open-label, investigator blinded Phase 2 clinical trial in non-active progressive MS patients. Enrollment concluded in January 2025 with topline results expected in the third quarter of 2025. We plan to work closely with regulatory health authorities from the FDA, European Medicines Agency and other international regulatory bodies, MS experts, and patient representatives to determine the proper path to advance CNM-Au8 into Phase 3 and potential future approval. The FDA has confirmed an end of Phase 2 meeting with us during the third quarter of 2025 to review results from the Phase 2 VISIONARY-MS trial and discuss a planned Phase 3 study focusing on cognition improvement as an adjunct to standard-of-care MS therapies, addressing a critical unmet medical need for people struggling with MS.
The chart below reflects the growing body of evidence for CSN therapeutics from our completed and ongoing clinical programs.
Recent Competition Update
Despite the great need for an effective disease-modifying treatment for ALS and significant research efforts by the pharmaceutical industry to meet this need, there have been limited clinical successes and no curative therapies approved to date. In early 2025, the topline results were announced for two regimens of the HEALEY ALS Platform Trial (ABBV-CLS-7262 from Calico Life Sciences LLC and AbbVie Inc., and DNL343 from Denali Therapeutics Inc.), with both treatments failing to meet their primary and key secondary endpoints.
Financial Overview
Our financial condition, results of operations, and the period-to-period comparability of our financial results are principally affected by the following factors:
Research and Development Expense
The discovery and development of novel drug candidates requires a significant investment of resources over a prolonged period of time, and a core part of our strategy is to continue making sustained investments in this area. As a result of this commitment, our pipeline of drug candidates has been advancing, with substantially all our research and development expenses relating to our lead asset, CNM-Au8.
Our research and development expenses are affected by the scope and advancement of our existing product pipeline and the commencement of new drug programs. Drug candidates in later stages of clinical development generally have higher development costs than those in earlier stages, primarily due to costs and fees for per patient clinical trial sites for larger clinical trials, opening and monitoring clinical sites, contract research organization (“CRO”) activity, and manufacturing. We anticipate that our research and development expenses will increase in future years if and when we advance our assets into Phase 3. Additionally, if we are able to file an NDA with the FDA under an accelerated approval pathway or subsequent to future Phase 3 clinical development activities, if any, we anticipate that our research and development expenses related to regulatory activities would increase in advance of receiving regulatory approval.
Research and development costs consist primarily of payroll and personnel expenses for salaries, benefits, and stock-based compensation; supplies, materials, and manufacturing expenses to support our clinical trials; payments to CROs, principal investigators, and clinical trial sites; costs of preclinical and nonclinical activities; consulting costs; and allocated overhead costs, including rent, equipment, utilities, depreciation, insurance, maintenance, and information technology. Research and development costs are charged to operations as incurred, and nonrefundable advance payments related to future research and development activities are initially recorded as assets and are expensed when we receive the related goods or services. Grant funding is recognized as a reduction in research and development costs.
Our clinical trial accrual process seeks to account for expenses resulting from obligations under contracts with CROs, consultants, and clinical sites in connection with conducting clinical trials. The financial terms of these contracts vary and may result in payment flows that do not match the periods over which materials or services are provided to us under such contracts. We reflect the appropriate clinical trial expenses in the condensed consolidated financial statements by matching the appropriate expenses with the period in which services are performed. In the event advance payments are made to CROs, the payments are recorded as prepaid assets and expensed over the period in which services are performed.
General and Administrative Expense
General and administrative expenses consist primarily of payroll and personnel expenses for salaries, benefits, and stock-based compensation; fees for legal, finance, accounting, tax, and information technology services; insurance costs; expenses for public and investor relations; rent, utilities, depreciation, and other costs related to our facilities.
We anticipate that our general and administrative expenses in future periods will be contingent upon our discussions with the FDA. If we are able to file an NDA with the FDA under an accelerated approval pathway, we anticipate our general and administrative expenses would increase in future periods to support increases in our drug development activities and as we build our commercial capabilities in advance of receiving regulatory approval. This potential increase will likely include increased headcount, increased stock-based compensation expenses, expanded infrastructure including certain sales and marketing activities performed ahead of regulatory approval, and increased insurance expenses. If we are unable to file an NDA with the FDA under an accelerated approval pathway, we would need to continue investing in clinical research activities and we anticipate our general and administrative expenses would decrease in future periods as we decrease commercial expansion projects, including at our Elkton, Maryland facility, and as we implement cost-saving initiatives, such as a reduction in compensation, a hiring freeze, and elimination of certain staff positions.
Total Other Income (Expense), Net
Total other income (expense), net, consists primarily of (i) interest income and interest expense, (ii) changes in the fair value of our common stock warrant liabilities, derivative liabilities, and Contingent Earn-outs, and (iii) research and development tax credits, unrestricted grants, and conditional grants for which applicable conditions have been met.
Results of Operations
Our results of operations for the three and six months ended June 30, 2025 and 2024 were as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||||||||||
| (in thousands) |
2025 |
2024 |
Change |
2025 |
2024 |
Change |
||||||||||||||||||
| Revenue: |
||||||||||||||||||||||||
| Product revenue |
$ | 1 | $ | 64 | (98 | )% | $ | 65 | $ | 108 | (40 | )% | ||||||||||||
| Royalty revenue |
26 | 27 | (4 | )% | 43 | 56 | (23 | )% | ||||||||||||||||
| Total revenue |
27 | 91 | (70 | )% | 108 | 164 | (34 | )% | ||||||||||||||||
| Operating expenses: |
||||||||||||||||||||||||
| Cost of revenue |
— | 18 | * | 20 | 34 | (41 | )% | |||||||||||||||||
| Research and development |
3,514 | 4,150 | (15 | )% | 4,995 | 10,019 | (50 | )% | ||||||||||||||||
| General and administrative |
2,377 | 3,314 | (28 | )% | 5,033 | 6,734 | (25 | )% | ||||||||||||||||
| Total operating expenses |
5,891 | 7,482 | (21 | )% | 10,048 | 16,787 | (40 | )% | ||||||||||||||||
| Loss from operations |
(5,864 | ) | (7,391 | ) | (21 | )% | (9,940 | ) | (16,623 | ) | (40 | )% | ||||||||||||
| Total other income (expense), net |
(1,555 | ) | 606 | * | 1,770 | (1,242 | ) | * | ||||||||||||||||
| Net loss |
$ | (7,419 | ) | $ | (6,785 | ) | 9 | % | $ | (8,170 | ) | $ | (17,865 | ) | (54 | )% | ||||||||
Revenue
Product revenue relates to our dietary supplement products and consists of (i) sales of an aqueous zinc-silver ion dietary (mineral) supplement sold by our wholly-owned subsidiary, dOrbital, Inc., under the trade name “rMetx™ ZnAg Immune Boost,” or under a supply agreement with 4Life under the trade name “Zinc Factor™,” and (ii) sales of KHC46, an aqueous gold dietary (mineral) supplement of very low-concentration, sold under a supply agreement with 4Life under the trade name “Gold Factor™.” Royalty revenue relates to our dietary supplement products and consists of proceeds under an exclusive and royalty-bearing license agreement with 4Life relating to the sale of Gold Factor. During the three and six months ended June 30, 2025 and 2024, changes in product and royalty revenues were due to the timing of purchases and sales of Zinc Factor and Gold Factor by 4Life under the supply and license agreements.
Cost of Revenue
Cost of revenue relates to production and distribution costs for the sales of Gold Factor, Zinc Factor, and rMetx dietary supplements.
Research and Development Expense
Research and development expense during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||||||||||
| (in thousands) |
2025 |
2024 |
Change |
2025 |
2024 |
Change |
||||||||||||||||||
| CNM-Au8: |
||||||||||||||||||||||||
| Amyotrophic lateral sclerosis |
$ | 1,468 | $ | 610 | 141 | % | $ | 2,811 | $ | 1,380 | 104 | % | ||||||||||||
| Multiple sclerosis |
164 | 69 | 138 | % | 189 | 161 | 17 | % | ||||||||||||||||
| Parkinsonʼs disease |
— | 2 | * | — | 2 | * | ||||||||||||||||||
| Regulatory activities |
130 | 122 | 7 | % | 260 | 462 | (44 | )% | ||||||||||||||||
| General/pre-clinical/non-clinical |
19 | 200 | (91 | )% | 82 | 328 | (75 | )% | ||||||||||||||||
| CNM-ZnAg |
— | — | * | — | 13 | * | ||||||||||||||||||
| Unallocated: |
||||||||||||||||||||||||
| Facilities |
386 | 401 | (4 | )% | 805 | 782 | 3 | % | ||||||||||||||||
| Depreciation |
337 | 347 | (3 | )% | 675 | 701 | (4 | )% | ||||||||||||||||
| Manufacturing |
187 | 422 | (56 | )% | 270 | 661 | (59 | )% | ||||||||||||||||
| Research |
2 | 141 | (99 | )% | 7 | 316 | (98 | )% | ||||||||||||||||
| Equipment |
14 | 35 | (60 | )% | 28 | 64 | (56 | )% | ||||||||||||||||
| Maintenance |
32 | 17 | 88 | % | 64 | 37 | 73 | % | ||||||||||||||||
| Information technology |
54 | 29 | 86 | % | 119 | 66 | 80 | % | ||||||||||||||||
| Other |
79 | 30 | 163 | % | 104 | 59 | 76 | % | ||||||||||||||||
| Personnel |
2,100 | 2,545 | (17 | )% | 4,260 | 5,209 | (18 | )% | ||||||||||||||||
| Stock-based compensation |
600 | 903 | (34 | )% | 1,546 | 1,780 | (13 | )% | ||||||||||||||||
| Grant revenue as a reduction of research and development expense |
(2,058 | ) | (1,723 | ) | 19 | % | (6,225 | ) | (2,002 | ) | 211 | % | ||||||||||||
| Total research and development |
$ | 3,514 | $ | 4,150 | (15 | )% | $ | 4,995 | $ | 10,019 | (50 | )% | ||||||||||||
| * |
Not meaningful. |
The change in research and development expenses was primarily due to the following:
| (i) |
an increase in expenses related to our lead drug candidate, CNM-Au8, primarily due to (A) an increase in expenses related to our ALS clinical programs, including our ACT-EAP due to increased enrollment in the EAP, and an increase in expenses for planning activities for our RESTORE-ALS clinical trial; partially offset by a decrease in expenses related to the HEALEY ALS Platform Trial due to the previous completion of the blinded and open-label extension portions of the trial and a decrease in expenses related to our two ongoing EAPs with Massachusetts General Hospital, (B) an increase in expenses related to our MS clinical programs primarily due to an increase in expenses for our MS EAP which began enrollment in September 2024, partially offset by a decrease in expenses related to our REPAIR-MS clinical trial due to the conclusion of enrollment of the ongoing second dosing cohort, (C) an increase in expenses for regulatory activities during the three months ended June 30, 2025 related to our ongoing FDA discussions and NDA submission-related activities, with a decrease in expenses for regulatory activities during the six months ended June 30, 2025 primarily driven by lower expenses related to NDA submission-related activities in the first quarter of 2025 compared to the same period in 2024, and (D) a decrease in pre-clinical, non-clinical, and other general CNM-Au8-related expenses; |
| (ii) |
a decrease in unallocated expenses, primarily due to: (A) a decrease in manufacturing expenses due to the conclusion of various clinical programs and (B) a decrease in expenses related to general research activities; partially offset by (D) an increase in information technology-related expenses and (F) an increase in other miscellaneous expenses; |
| (iii) |
a decrease in personnel expenses, primarily due to cost-saving initiatives and a decrease in expenses for manufacturing personnel due to the conclusion of various clinical programs; |
| (iv) |
a decrease in stock-based compensation expense, primarily due to the timing of award grants, vesting, and forfeitures for research and development personnel; and |
| (v) |
an increase in grant revenue, recorded as a reduction to research and development expense, due to an increase in enrollment and study operations in the ACT-EAP which resulted in higher reimbursable expenses during the six months ended June 30, 2025, partially offset by a decrease in grant revenue related to our REPAIR-MS clinical trial due to the conclusion of enrollment of the ongoing second dosing cohort. |
General and Administrative Expense
General and administrative expense during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||||||||||
| (in thousands) |
2025 |
2024 |
Change |
2025 |
2024 |
Change |
||||||||||||||||||
| Insurance |
$ | 181 | $ | 187 | (3 | )% | $ | 362 | $ | 373 | (3 | )% | ||||||||||||
| Legal |
175 | 284 | (38 | )% | 323 | 359 | (10 | )% | ||||||||||||||||
| Finance and accounting |
220 | 124 | 77 | % | 530 | 373 | 42 | % | ||||||||||||||||
| Public and investor relations |
119 | 199 | (40 | )% | 230 | 433 | (47 | )% | ||||||||||||||||
| Facilities |
31 | 31 | 0 | % | 61 | 63 | (3 | )% | ||||||||||||||||
| Depreciation |
29 | 67 | (57 | )% | 95 | 133 | (29 | )% | ||||||||||||||||
| Information technology |
47 | 87 | (46 | )% | 96 | 166 | (42 | )% | ||||||||||||||||
| Personnel |
788 | 1,044 | (25 | )% | 1,620 | 2,140 | (24 | )% | ||||||||||||||||
| Stock-based compensation |
767 | 1,048 | (27 | )% | 1,768 | 2,184 | (19 | )% | ||||||||||||||||
| Grant revenue as a reduction of general and administrative expense |
(65 | ) | (106 | ) | (39 | )% | (228 | ) | (106 | ) | 115 | % | ||||||||||||
| Other |
85 | 349 | (76 | )% | 176 | 616 | (71 | )% | ||||||||||||||||
| Total general and administrative |
$ | 2,377 | $ | 3,314 | (28 | )% | $ | 5,033 | $ | 6,734 | (25 | )% | ||||||||||||
The change in general and administrative expense was primarily due to the following:
| (i) |
a decrease in legal fees, primarily due to a decrease in legal fees related to intellectual property and regulatory activities; partially offset by an increase in legal fees related to financing and fundraising and other general corporate legal fees; |
| (ii) |
an increase in finance and accounting fees, primarily due to an increase in audit and tax fees and fees from consultants, advisors, and other financial vendors; |
| (iii) |
a decrease in fees related to our public and investor relations efforts; |
| (iv) |
a decrease in information technology-related expenses; |
| (v) |
a decrease in personnel expenses, primarily due to cost-saving initiatives; |
| (vi) |
a decrease in stock-based compensation expense, primarily due to the timing of award grants, vesting, and forfeitures for general and administrative personnel; |
| (vii) | a decrease in grant revenue related to the ACT-EAP during the three months ended June 30, 2025, recorded as a reduction to general and administrative expense, due to higher grant revenue during the three months ended June 30, 2024, as reimbursements for expenses incurred from September 2023 to March 2024 were not recognized until we entered into an agreement covering the first year of the ACT-EAP in April 2024 and grant recognition criteria were met; and an increase in grant revenue during the six months ended June 30, 2025 due to an increase in enrollment and study operations in the ACT-EAP which resulted in higher reimbursable expenses; and |
| (viii) |
a decrease in other expenses during the three months ended June 30, 2025 due to a decrease in expenses related to lobbying activities, travel, meals, office, and other miscellaneous expenses. |
Total Other Income (Expense), Net
Total other income (expense), net, during the three and six months ended June 30, 2025 and 2024 was as follows:
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||||||||||
| (in thousands) |
2025 |
2024 |
Change |
2025 |
2024 |
Change |
||||||||||||||||||
| Interest income |
$ | 62 | $ | 269 | (77 | )% | $ | 143 | $ | 628 | (77 | )% | ||||||||||||
| Interest expense |
(679 | ) | (1,282 | ) | (47 | )% | (1,287 | ) | (2,526 | ) | (49 | )% | ||||||||||||
| Change in fair value of common stock warrant liabilities |
(515 | ) | 1,568 | * | 1,995 | 259 | 670 | % | ||||||||||||||||
| Change in fair value of derivative liabilities |
(439 | ) | — | * | 708 | — | * | |||||||||||||||||
| Change in fair value of Clene Nanomedicine contingent earn-out liability |
— | 22 | * | — | 75 | * | ||||||||||||||||||
| Change in fair value of Initial Stockholders contingent earn-out liability |
— | 3 | * | — | 10 | * | ||||||||||||||||||
| Research and development tax credits and unrestricted grants |
16 | 26 | (38 | )% | 211 | 312 | (32 | )% | ||||||||||||||||
| Total other income (expense), net |
$ | (1,555 | ) | $ | 606 | * | $ | 1,770 | $ | (1,242 | ) | * | ||||||||||||
| * |
Not meaningful. |
The change in total other income (expense), net, was primarily due to the following:
| (i) |
a decrease in interest income primarily due to lower average balances of cash and cash equivalents and lower interest rates in 2025; |
| (ii) |
a decrease in interest expense primarily due to declining balances of notes payable following principal repayments, a decrease in amortization of debt discounts on notes payable, and a decrease in non-cash interest expense on notes payable; |
| (iii) |
a loss from the changes in fair value of the 2023 Avenue Warrant, Tranche A Warrants, and 2024 Common Warrants during the three months ended June 30, 2025, and a gain during the six months ended June 30, 2025. The changes in fair value were due to changes in price of our Common Stock on Nasdaq and updates in valuation model assumptions (see “Critical Accounting Estimates”); |
| (iv) | a loss from the change in fair value of the derivative liabilities separated from our senior secured convertible promissory notes (the “2024 SSCP Notes”) during the three months ended June 30, 2025, and a gain during the six months ended June 30, 2025. The changes in fair value were due to changes in price of our Common Stock on Nasdaq and updates in valuation model assumptions (see “Critical Accounting Estimates”); |
| (ix) |
a gain from the change in fair value of the Clene Nanomedicine Contingent Earn-out liability and Initial Stockholders Contingent Earn-out liability during the three and six months ended June 30, 2024. The changes were due to changes in price of our Common Stock on Nasdaq and updates in valuation model assumptions; and |
| (x) |
a decrease in research and development tax credits and unrestricted grants due to changes in the amount of qualifying research and development expenses incurred. |
Taxation
United States
We are incorporated in the state of Delaware and subject to statutory U.S. federal corporate income tax at a rate of 21.00%. We are also subject to state income tax in Maryland at a rate of 8.25%, and in Utah at a rate of 4.55% and 4.65% for the six months ended June 30, 2025 and 2024, respectively. As of June 30, 2025 and December 31, 2024, we recorded a full valuation allowance against our net deferred tax assets due to the uncertainty as to whether such assets will be realized resulting from our three-year cumulative loss position and the uncertainty surrounding our ability to generate pre-tax income in the foreseeable future.
Australia
Our wholly-owned subsidiary, Clene Australia Pty Ltd (“Clene Australia”), was established in Australia in March 2018 and is subject to corporate income tax at a rate of 30.00%. Clene Australia had no taxable income or provision for income taxes for the six months ended June 30, 2025 and 2024. We recorded other income of $40,000 and $40,000 for the six months ended June 30, 2025 and 2024, respectively, for research and development tax credits pertaining to Clene Australia for the 2025 and 2024 tax years, respectively.
Netherlands
Our wholly-owned subsidiary, Clene Netherlands B.V. (“Clene Netherlands”), was established in the Netherlands in April 2021 and is subject to corporate income tax at a rate of 19.00% up to €200,000 of taxable income and 25.80% for taxable income in excess of €200,000 for the six months ended June 30, 2025 and 2024. Clene Netherlands had no taxable income or provision for income taxes for the six months ended June 30, 2025 and 2024.
Liquidity and Capital Resources
Sources of Capital
We have incurred significant losses and negative cash flows from operations since our inception. We expect to incur additional losses in the future to fund our operations and conduct research and development of our drug candidates. We recognize the need to raise additional capital to fully implement our business plan. The long-term continuation of our business plan is dependent upon the generation of sufficient revenues from our products to offset expenses and capital expenditures. In the event that we do not generate sufficient revenues and are unable to obtain funding, we will be forced to delay, reduce, or eliminate some or all of our research and development programs, product portfolio expansion, commercialization efforts, or capital expenditures, which could adversely affect our business prospects, ability to meet long-term liquidity needs, or we may be unable to continue operations.
Since our inception, we have dedicated substantially all our resources to the development of our drug candidates. We have financed our operations principally through the following sources:
| ● | gross proceeds of $192.1 million from equity financing, including sales of common stock, preferred stock, common stock warrants, and pre-funded common stock warrants; |
| ● | gross proceeds of $69.6 million from borrowings under notes payable, convertible notes payable, and convertible promissory notes; |
| ● | gross proceeds of $9.4 million from the Reverse Recapitalization; |
| ● | gross proceeds of $10.1 million from refundable research and development tax credits; |
| ● | gross proceeds of $11.6 million from grants from various organizations; and |
| ● | gross proceeds of $1.1 million from stock option and warrant exercises. |
We also received indirect financial support for the HEALEY ALS Platform Trial, administered by Massachusetts General Hospital, which conducted an ALS platform trial of CNM-Au8 alongside multiple other drug candidates, at significantly lower costs than we would have otherwise incurred if we had conducted a comparably designed clinical trial at reasonable market rates.
Going Concern
We incurred a loss from operations of $5.9 million and $7.4 million for the three months ended June 30, 2025 and 2024, respectively; and $9.9 million and $16.6 million for the six months ended June 30, 2025 and 2024, respectively. Our accumulated deficit was $290.3 million and $282.1 million as of June 30, 2025 and December 31, 2024, respectively. Our cash and cash equivalents totaled $7.3 million and $12.2 million as of June 30, 2025 and December 31, 2024, respectively, and net cash used in operating activities was $9.8 million and $13.4 million for the six months ended June 30, 2025 and 2024, respectively.
We have incurred significant losses and negative cash flows from operations since our inception. We have not generated significant revenues since our inception, and we do not anticipate generating significant revenues unless we successfully complete development and obtain regulatory approval for commercialization of a drug candidate. We expect to incur additional losses in the future, particularly as we advance the development of our clinical-stage drug candidates, continue research and development of our preclinical drug candidates, and initiate additional clinical trials of, and seek regulatory approval for, these and other future drug candidates. We expect that within the next twelve months, we will not have sufficient cash and other resources on hand to sustain our current operations or meet our obligations as they become due unless we obtain additional financing. Additionally, pursuant to our senior secured convertible promissory notes (the “2024 SSCP Notes”), we are required to maintain unrestricted cash and cash equivalents of at least $2.0 million to avoid acceleration of the full balance of the 2024 SSCP Notes (see Note 8 to the condensed consolidated financial statements). These conditions raise substantial doubt about the Company’s ability to continue as a going concern.
To mitigate our funding needs, we plan to raise additional funding, including exploring equity financing and offerings, debt financing, licensing or collaboration arrangements with third parties, as well as utilizing our existing at-the-market facility and equity purchase agreement and potential proceeds from the exercise of outstanding warrants and stock options. These plans are subject to market conditions and reliance on third parties, and there is no assurance that effective implementation of our plans will result in the necessary funding to continue current operations. During the three and six months ended June 30, 2025, we generated $2.3 million and $5.1 million, respectively, of gross proceeds from our equity distribution agreement and subsequent to June 30, 2025, we generated $1.9 million of gross proceeds from our equity distribution agreement and we raised $1.5 million from the issuance of senior secured convertible promissory notes. We have implemented cost-saving initiatives, including delaying and reducing certain research and development programs and commercialization efforts, reducing employee compensation, and elimination of certain staff positions. We have concluded that our plans do not alleviate the substantial doubt about our ability to continue as a going concern beyond one year from the date the condensed consolidated financial statements are issued.
The accompanying condensed consolidated financial statements have been prepared assuming we will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. As a result, the accompanying condensed consolidated financial statements do not include any adjustments relating to the recoverability and classification of assets and their carrying amounts, or the amounts and classification of liabilities that may result should we be unable to continue as a going concern.
Short-Term Material Cash Requirements
For at least the next twelve months, our primary capital requirements are to fund our operations, including research and development, personnel, regulatory, and other clinical trial costs related to development of our lead drug candidate, CNM-Au8; general and administrative costs to support our drug development and pre-commercial activities in advance of receiving regulatory approval for our drug candidates; and principal and interest payments on our notes payable and convertible notes payable. Firm commitments for funds include approximately $1.4 million of payments under operating lease obligations, payment of principal and interest on notes payable and convertible notes payable totaling $0.7 million, and a commitment for capital expenditures totaling $0.2 million related to the construction of our manufacturing facilities. We expect to meet our short-term liquidity requirements primarily through cash on hand. Additional sources of funds include equity financing, debt financing, or other capital sources.
We enter into agreements in the normal course of business with CROs for clinical trials and with vendors for preclinical studies and other services and products for operating purposes, which are cancelable at any time by us, subject to payment of our remaining obligations under binding purchase orders and, in certain cases, nominal early termination fees. These commitments are not deemed significant.
Long-Term Material Cash Requirements
Beyond the next twelve months, our primary capital requirements are to fund our operations, including research and development, personnel, regulatory, and other clinical trial costs related to development of our lead drug candidate, CNM-Au8; general and administrative costs to support our drug development activities in advance of receiving regulatory approval for our drug candidates; and principal and interest payments on our notes payable and convertible notes payable. Additional funds may be spent to initiate new clinical trials, at our discretion. Known obligations beyond the next twelve months include $4.5 million of payments under operating lease obligations, and interest and principal repayment of notes payable and convertible notes payable of $18.3 million. We expect to meet our long-term liquidity requirements primarily through equity financing, debt financing, or other capital sources.
Use of Funds
Our cash flows for the six months ended June 30, 2025 and 2024 were as follows:
| Six Months Ended June 30, |
||||||||
| (in thousands) |
2025 |
2024 |
||||||
| Net cash used in operating activities |
$ | (9,755 | ) | $ | (13,438 | ) | ||
| Net cash provided by investing activities |
— | 6,319 | ||||||
| Net cash provided by financing activities |
4,806 | 9 | ||||||
| Effect of foreign exchange rate changes on cash |
79 | (29 | ) | |||||
| Net decrease in cash, cash equivalents and restricted cash |
$ | (4,870 | ) | $ | (7,139 | ) | ||
Our primary use of cash in all periods presented was to fund our research and development, regulatory and other clinical trial costs, and general corporate expenditures.
Operating Activities
Net cash used in operating activities was $9.8 million for the six months ended June 30, 2025, which resulted from a net loss of $8.2 million, adjusted for non-cash items totaling $2.2 million and a net change in operating assets and liabilities of $3.8 million. Significant non-cash items included: (i) depreciation expense of $0.8 million related to laboratory and office equipment and leasehold improvements, (ii) non-cash lease expense of $0.3 million, (iii) stock-based compensation expense of $3.3 million, (iv) accretion of debt discount of $0.5 million, (v) non-cash interest expense on notes payable of $24,000, (vi) a change in fair value of our common stock warrant liabilities of $2.0 million due to changes in the price of our Common Stock on Nasdaq and changes in valuation model inputs, and (vii) a change in fair value of our derivative liabilities of $0.7 million due to changes in the price of our Common Stock on Nasdaq and changes in valuation model inputs. The net change in operating assets and liabilities was primarily attributable to: (A) a decrease in accounts receivable of $0.1 million and a decrease in accounts payable of $0.4 million due to the timing of vendor invoicing and payments, (B) an increase in prepaid expenses and other current assets of $0.8 million due to the timing of vendor invoicing and payments, the timing of receipt of metals to be used in research and development, and an increase in research and development tax credits receivable, partially offset by a decrease in prepaid clinical and CRO expenses related to the ACT-EAP, (C) a decrease in accrued liabilities of $2.3 million primarily due to a decrease in deferred grants and a decrease in other miscellaneous accrued liabilities, partially offset by an increase in accrued compensation and benefits, and (D) a decrease in operating lease obligations of $0.3 million.
Net cash used in operating activities was $13.4 million for the six months ended June 30, 2024, which resulted from a net loss of $17.9 million, adjusted for non-cash items totaling $5.4 million and a net change in operating assets and liabilities of $0.9 million. Significant non-cash items included: (i) depreciation expense of $0.8 million related to laboratory and office equipment and leasehold improvements, (ii) non-cash lease expense of $0.3 million, (iii) stock-based compensation expense of $4.0 million, (iv) accretion of debt discount of $0.8 million, (v) non-cash interest expense of $28,000, (vi) non-cash interest income on marketable securities of $0.2 million, (vii) a change in fair value of our common stock warrant liabilities of $0.3 million due to changes in the price of our Common Stock on Nasdaq and changes in valuation model inputs, and (viii) a change in fair value of the Clene Nanomedicine and Initial Stockholders Contingent Earn-outs of $0.1 million and $10,000, respectively, due to changes in the price of our Common Stock on Nasdaq and changes in valuation model inputs. The net change in operating assets and liabilities was primarily attributable to: (A) a decrease in accounts receivable of $0.1 million and a decrease in accounts payable of $0.4 million due to the timing of vendor invoicing and payments, (B) an increase in prepaid expenses and other current assets of $2.5 million due to the timing of vendor invoicing and payments, the timing of receipt of metals to be used in research and development, an increase in prepaid ACT-EAP expenses, and an increase in research and development tax credits receivable, (C) an increase in accrued liabilities of $2.2 million primarily due to increased accrued compensation and benefits and increased deferred grants, partially offset by a decrease in accrued CRO and clinical fees, and (D) a decrease in operating lease obligations of $0.3 million.
Investing Activities
We had no net cash provided by or used in investing activities for the six months ended June 30, 2025. Net cash provided by investing activities was $6.3 million for the six months ended June 30, 2024, which consisted of proceeds from maturities of marketable securities of $12.5 million, partially offset by purchases of marketable securities of $6.2 million and purchases of property and equipment of $13,000.
Financing Activities
Net cash provided by financing activities was $4.8 million for the six months ended June 30, 2025, which consisted of proceeds from the issuance of common stock of $5.0 million, partially offset by payments of notes payable of $0.2 million. Net cash used in financing activities was $9,000 for the six months ended June 30, 2024, which consisted of proceeds from the exercise of stock options of $36,000, partially offset by payments of finance lease obligations of $27,000.
Public Offerings
In October 2024, pursuant to a placement agency agreement with Canaccord Genuity LLC (“Canaccord”), we sold 725,000 shares of Common Stock and pre-funded warrants to purchase up to 17,626 shares of Common Stock at an exercise price of $0.001 per share. The aggregate gross proceeds were approximately $3.5 million, excluding the proceeds, of any, from the exercise of the pre-funded warrants and before deducting placement agent fees and expenses and other expenses payable by us. We paid Canaccord a placement agent fee of 6.00% of the aggregate gross proceeds of the offering. The offering was made pursuant to our registration statement on Form S-3 (file number 333-264299), declared effective by the Securities and Exchange Commission (“SEC”) on April 26, 2022, and a related prospectus supplement. Additionally, in separate, concurrent private placements, we also sold 379,930 shares of Common Stock, pre-funded warrants to purchase up to 424,358 shares of Common Stock at an exercise price of $0.001 per share, and warrants to purchase up to 1,546,914 shares of Common Stock at an exercise price of $4.82 per share. The aggregate gross proceeds from the private placements were approximately $3.8 million, of which $1.3 million was contributed by certain of our directors, executive officers and their affiliated entities, and excludes the proceeds, if any, from the exercise of the warrants and pre-funded warrants.
Common Stock Sales Agreement
During the three and six months ended June 30, 2025, we sold 758,990 and 1,337,195 shares of Common Stock, respectively, under our April 2022 equity distribution agreement (the “2022 ATM Agreement”) and April 2025 equity distribution agreement (the “2025 ATM Agreement,” and collectively with the 2022 ATM Agreement, the “ATM Agreements”) with Canaccord, generated gross proceeds of $2.3 million and $5.1 million, respectively, and paid commissions of $35,000 and $0.1 million, respectively. We did not effect any sales during any of the other periods presented herein. The issuance and sale of Common Stock by us under the 2022 ATM Agreement was made pursuant to our registration statement on Form S-3 (file number 333-264299), declared effective by the SEC on April 26, 2022, and a related prospectus supplement, which expired on April 26, 2025. The issuance and sale of Common Stock by us under the 2025 ATM Agreement was made pursuant to our registration statement on Form S-3 (file number 333-286058), declared effective by the SEC on April 25, 2025, and a related prospectus supplement.
Critical Accounting Estimates
Our discussion and analysis of our financial condition and results of operations is based on our condensed consolidated financial statements, which have been prepared in accordance with U.S. Generally Accepted Accounting Principles. The preparation of these condensed consolidated financial statements requires us to make estimates, assumptions, and judgments that affect the reported amounts of assets, liabilities, revenues, costs, and expenses. We evaluate our estimates and judgments on an ongoing basis, and our actual results may differ from these estimates. We base our estimates on historical experience, known trends and events, contractual milestones, and other various factors that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources.
We consider the following estimates to be critical as they involve a significant level of estimation uncertainty and have had or are reasonably likely to have a material impact on our financial condition and results of operations.
Convertible Notes
In accordance with ASU 2020-06, Debt—Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic 815-40): Accounting for Convertible Instruments and Contracts in an Entity’s Own Equity, we classified the 2022 DHCD Loan as convertible notes payable in the condensed consolidated balance sheets and did not separate the conversion option from the host contract as it did not meet the requirements for accounting as a derivative instrument. We account for the convertible note as a single liability measured at its amortized cost as of June 30, 2025 and December 31, 2024, with a carrying value of $5.3 million and $5.3 million, respectively.
We classified a portion of the 2024 SSCP Notes as convertible notes payable in the consolidated balance sheets and separated three features from the host contract as derivative instruments measured at fair value: (i) the conversion option (the “SSCPN Conversion Feature”), (ii) the redemption option upon a change of control or any bankruptcy, liquidation, or other restructuring process consisting of a cash payment equal to 115% of the outstanding principal (the “SSCPN Redemption Feature”), and (iii) the acceleration option plus a penalty equal to 10% of all outstanding principal and accrued and unpaid interest upon the occurrence and continuation of certain events of default (the “SSCPN Default Feature,” collectively with the SSCPN Conversion Feature and SSCPN Redemption Feature, the “SSCPN Derivative Liabilities”). We accounted for the remainder of the 2024 SSCP Notes as liabilities measured at their amortized cost as of June 30, 2025 and December 31, 2024, with a carrying value of $9.0 million and $8.6 million, respectively. We remeasure the SSCPN Derivative Liabilities at each reporting date and record the change in fair value as a component of other income (expense), net in the condensed consolidated statements of operations and comprehensive loss. During the three and six months ended June 30, 2025, the change in fair value of the SSCPN Derivative Liabilities resulted in a loss of $0.4 million and a gain of $0.7 million, respectively. We estimate the fair value of the 2024 SSCP Notes with and without the SSCPN Derivative Liabilities and calculate the difference as the implied fair value of the SSCPN Derivative Liabilities. The valuation model consists of a discounted cash flow model and a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) a change of control transaction, (ii) dissolution of the Company, or (iii) another outcome outside of (i)-(ii). These estimates require significant judgment. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
104.20 | % | 101.50 | % | ||||
| Risk-free interest rate |
4.00% – 4.30 | % | 4.20 | % | ||||
| Expected dividend yield |
0.00 | % | 0.00 | % | ||||
| Expected term (in years) |
0.33 – 0.97 | 0.50 – 1.47 | ||||||
| Probability of change of control |
20.00 | % | 10.00 | % | ||||
| Probability of dissolution |
45.00 | % | 45.00 | % | ||||
| Probability of other outcome |
35.00 | % | 45.00 | % | ||||
Common Stock Warrant Liabilities
In accordance with ASC 815, we recognized the below common stock warrants as derivative liabilities measured at fair value and will remeasure them at each reporting date and record the change in fair value as a component of other income (expense), net, in the condensed consolidated statements of operations and comprehensive loss.
Pursuant to amendments to the 2021 Avenue Loan in June 2023 and September 2024, we issued a warrant to purchase 150,000 shares of Common Stock at $4.6014 per share (the “2023 Avenue Warrant”). The change in fair value of the 2023 Avenue Warrant resulted in a loss of $25,000 and a gain of $0.1 million during the three months ended June 30, 2025 and 2024, respectively; and a gain of $0.1 million and a loss of $0.1 million during the six months ended June 30, 2025 and 2024, respectively. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) settlement of the instrument upon a change of control transaction, (ii) dissolution of the Company, or (iii) another outcome outside of (i)-(ii). These estimates require significant judgment. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
96.50% – 99.20 | % | 100.20% – 101.40 | % | ||||
| Risk-free interest rate |
3.70% – 4.20 | % | 4.20% – 4.30 | % | ||||
| Expected dividend yield |
0.00 | % | 0.00 | % | ||||
| Expected term (in years) |
0.67 – 3.00 | 0.75 – 3.50 | ||||||
| Probability of change of control |
20.00 | % | 10.00 | % | ||||
| Probability of dissolution |
45.00 | % | 45.00 | % | ||||
| Probability of other outcome |
35.00 | % | 45.00 | % | ||||
Pursuant to an underwritten public offering in June 2023, we issued the Tranche A Warrants to purchase 2,500,000 shares of Common Stock at $22.00 per share. The change in fair value of the Tranche A Warrants resulted in a loss of $30,000 and a gain of $1.5 million during the three months ended June 30, 2025 and 2024, respectively; and a gain of $0.6 million and a gain of $0.3 million during the six months ended June 30, 2025 and 2024, respectively. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) FDA acceptance of an NDA for CNM-Au8, (ii) settlement upon a fundamental transaction, (iii) dissolution of the Company, and (iv) another outcome outside of (i)-(iii). These estimates require significant judgment. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
96.30% – 104.30 | % | 97.80% – 101.90 | % | ||||
| Risk-free interest rate |
4.00% – 4.40 | % | 4.20 | % | ||||
| Expected dividend yield |
0.00 | % | 0.00 | % | ||||
| Expected term (in years) |
0.29 – 0.96 | 0.71 – 1.46 | ||||||
| Probability of NDA acceptance |
20.00 | % | 20.00 | % | ||||
| Probability of fundamental transaction |
20.00 | % | 10.00 | % | ||||
| Probability of dissolution |
45.00 | % | 45.00 | % | ||||
| Probability of other outcome |
15.00 | % | 25.00 | % | ||||
Pursuant to a registered direct public offering in October 2024, we issued the 2024 Common Warrants to purchase 1,546,914 shares of Common Stock at $4.82 per share. The change in fair value of the 2024 Common Warrants resulted in a loss of $0.5 million and a gain of $1.3 million during the three and six months ended June 30, 2025, respectively. We estimate the fair value using a Black-Scholes option-pricing model with probability weights for the occurrence of the following events: (i) dissolution of the Company and (ii) another outcome outside of (i). These estimates require significant judgment. The unobservable valuation inputs were as follows:
| June 30, |
December 31, |
|||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
99.60 | % | 107.50 | % | ||||
| Risk-free interest rate |
3.70 | % | 4.40 | % | ||||
| Expected dividend yield |
0.00 | % | 0.00 | % | ||||
| Expected term (in years) |
4.25 | 4.75 | ||||||
| Probability of dissolution |
45.00 | % | 45.00 | % | ||||
| Probability of other outcome |
55.00 | % | 55.00 | % | ||||
Income Taxes
We account for uncertainty in income taxes by applying a two-step process to determine the amount of tax benefit to be recognized in the condensed consolidated financial statements. First, the tax position is evaluated to determine the likelihood that it will be sustained upon external examination by the taxing authorities. If the tax position is deemed more-likely-than-not to be sustained, the tax position is then assessed to determine the amount of benefit to recognize. The amount of the benefit that may be recognized is the largest amount that has a greater than 50% likelihood of being realized upon ultimate settlement. Additionally, we assess the likelihood that our deferred tax assets will be recovered from future taxable income and, to the extent we believe, based upon the weight of available evidence, that it is more likely than not that all or a portion of the deferred tax assets will not be realized, a valuation allowance is established through a charge to income tax expense. Potential for recovery of deferred tax assets is evaluated by estimating the future taxable profits expected and considering prudent and feasible tax planning strategies. The estimation of these factors requires significant judgment. Based on our evaluation of these factors, we have not recorded income tax benefits for the net operating losses or for research and development tax credits or other deferred tax assets due to uncertainty of realizing benefits from these items.
Stock-Based Compensation
We account for stock-based compensation arrangements using a fair value-based method for costs related to all share-based payments including stock options and stock awards. The fair value is recognized over the period during which a grantee was required to provide services in exchange for the option award and service-based stock awards, known as the requisite service period (usually the vesting period), on a straight-line basis. For stock awards with market conditions, the fair value is recognized over the period based on the expected milestone achievement dates as the derived service period (usually the vesting period), on a straight-line basis. For stock awards with performance conditions, the grant-date fair value of these awards is the market price on the applicable grant date, and compensation expense will be recognized when the conditions become probable of being satisfied. We will recognize a cumulative true-up adjustment once the conditions become probable of being satisfied as the related service period had been completed in a prior period. We elect to account for forfeitures as they occur, rather than estimating expected forfeitures.
We estimate the fair value of stock options using a Black-Scholes option-pricing model, which requires significant judgment. The unobservable inputs include the expected price volatility, risk-free interest rate, expected dividend yield, and expected term. The unobservable valuation inputs were as follows:
| Six Months Ended June 30, |
||||||||
| 2025 |
2024 |
|||||||
| Expected stock price volatility |
103.78% – 110.25 | % | 97.78% – 110.82 | % | ||||
| Risk-free interest rate |
4.05% – 4.24 | % | 4.04% – 4.58 | % | ||||
| Expected dividend yield |
0.00 | % | 0.00 | % | ||||
| Expected term of options (in years) |
5.00 – 6.25 | 5.00 – 10.00 | ||||||
We estimate the fair value of restricted stock awards using a Monte Carlo valuation model to simulate the achievement of certain stock price milestones. The unobservable inputs include the expected stock price volatility, risk-free interest rate, and expected term. No restricted stock awards were granted during the six months ended June 30, 2025 and 2024.
Item 3. Quantitative and Qualitative Disclosures About Market Risk
As a smaller reporting company, we are not required to provide information required by this Item.
Item 4. Controls and Procedures
Evaluation of Disclosure Controls and Procedures
Under the supervision and with the participation of management, including our principal executive officer and principal financial officer, we conducted an evaluation of the effectiveness of our disclosure controls and procedures as of June 30, 2025, as such term is defined in Rules 13a-15(e) and 15d-15(e) of the Securities Exchange Act of 1934 (the “Exchange Act”). As a result of this evaluation, our principal executive officer and principal financial officer have concluded that, as of June 30, 2025, our disclosure controls and procedures were not effective due to the material weaknesses in internal control over financial reporting described below. Notwithstanding the identified material weaknesses, management, including our principal executive officer and principal financial officer, believes the condensed consolidated financial statements included in this Quarterly Report on Form 10-Q fairly represent, in all material respects, our financial condition, results of operations and cash flows as of and for the periods presented in accordance with United States Generally Accepted Accounting Principles.
Disclosure controls and procedures are designed to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in the SEC rules and forms, and that such information is accumulated and communicated to our management, including our principal executive officer and principal financial officer, as appropriate to allow timely decisions regarding required disclosure.
Material Weaknesses in Internal Control over Financial Reporting
In connection with the audit of our financial statements as of and for the years ended December 31, 2024 and 2023, our management identified material weaknesses in our internal control over financial reporting. A material weakness is a deficiency, or combination of deficiencies, in internal control over financial reporting, such that there is a reasonable possibility that a material misstatement of our annual or interim financial statements will not be prevented or detected on a timely basis. The material weaknesses identified relate to the fact that we did not design or maintain an effective control environment commensurate with our financial reporting requirements. This deficiency in our control environment contributed to the following additional material weaknesses related to control activities and information and communication within our internal control over financial reporting:
| ● | we did not design and maintain controls over the preparation and review of reconciliations and the review and segregation of duties over manual journal entries, including controls over the completeness and accuracy of information; and |
| ● | we did not design and maintain information technology (“IT”) general controls for IT systems that are relevant to the preparation of the financial statements. Specifically, we did not design and maintain: (a) user access controls to ensure appropriate segregation of duties and that adequately restrict user and privileged access to financial applications, programs, and data to our appropriate personnel; (b) program change management controls to ensure that IT program and data changes affecting financial IT applications and underlying accounting records are identified, tested, authorized, and implemented appropriately; (c) computer operations controls to ensure that data backups are authorized and monitored; and (d) testing and approval controls for program development to ensure that new software development is aligned with business and IT requirements. |
Each of the control deficiencies described above could result in a misstatement of one or more account balances or disclosures that would result in a material misstatement to the annual or interim consolidated financial statements that would not be prevented or detected. Accordingly, our management has determined that each of the control deficiencies described above constitute material weaknesses.
Material Weakness Remediation
Management continues to be actively engaged and committed to taking the steps necessary to remediate the control deficiencies that constituted the above material weaknesses. During 2024, we made the following enhancements to our control environment:
| ● | we continued to strengthen the experience of our internal accounting team through refinement of our processes and internal controls over financial reporting and our IT and technical accounting resources; and |
| ● | until we have sufficient technical accounting resources, we engaged external consultants to provide support and to assist us in our evaluation of more complex applications of GAAP. |
Our remediation activities are continuing during 2025. In addition to the above actions, we expect to engage in additional activities, or have completed additional activities, including, but not limited to:
| ● | adding more technical accounting resources to enhance our control environment; and |
| ● | until we have sufficient technical accounting resources, engaging external consultants to provide support and to assist us in our evaluation of more complex applications of GAAP. |
We continue to enhance corporate oversight over process-level controls and structures to ensure that there is appropriate assignment of authority, responsibility, and accountability to enable remediation of our material weaknesses. We believe that our remediation plan will be sufficient to remediate the identified material weaknesses and strengthen our internal control over financial reporting. As we continue to evaluate, and work to improve, our internal control over financial reporting, management may determine that additional measures to address control deficiencies or modifications to the remediation plan are necessary.
Changes in Internal Control over Financial Reporting
Other than changes described under “—Material Weakness Remediation,” there were no changes in our internal control over financial reporting during the quarter ended June 30, 2025, that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
PART II—OTHER INFORMATION
Item 1. Legal Proceedings
We are not currently a party to any material pending legal proceedings. From time to time, we may, however, be involved in legal proceedings in the ordinary course of business. We cannot predict the outcome of any such legal proceedings, and despite the potential outcomes, the existence thereof may have an adverse impact on us because of defense and settlement costs, diversion of management resources and other factors.
Item 1A. Risk Factors
Our business, financial condition, and results of operations can be affected by a number of factors, whether currently known or unknown, including, but not limited to, those described in Part I, Item 1A, Risk Factors of our 2024 Annual Report on Form 10-K, which was filed with the SEC on March 24, 2025. Except for the risk factor disclosed in Part II, Item 1A, Risk Factors, of our Quarterly Report on Form 10-Q for the period ended March 31, 2025, which was filed with the SEC on May 7, 2025, there have been no material changes to the risk factors since previously disclosed in the 2024 Annual Report on Form 10-K. Any one or more of these factors could, directly or indirectly, cause our actual financial condition and results of operations to vary materially from past, or from anticipated future, financial condition and results of operations. Any of these factors, in whole or in part, could materially and adversely affect our business, financial condition, results of operations, and stock price.
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds
| (a) |
Recent Sales of Unregistered Securities |
None.
| (b) |
Use of Proceeds |
None.
| (c) |
Purchases of Equity Securities by the Issuer and Affiliated Purchasers |
None.
Item 3. Defaults Upon Senior Securities
None.
Item 4. Mine Safety Disclosures
Not Applicable.
Item 5. Other Information
During the three months ended June 30, 2025, of our officers or directors adopted or terminated any “Rule 10b5-1 trading arrangement” or any “non-Rule 10b5-1 trading arrangement,” as each term is defined in Item 408 of Regulation S-K.
Item 6. Exhibits
| Exhibit Number |
Exhibit Description |
|
| 3.1 |
Fourth Amended and Restated Certificate of Incorporation of Clene Inc. (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed by the registrant on May 11, 2023). |
|
| 3.2 | Certificate of Amendment to the Fourth Amended and Restated Certificate of Incorporation of Clene Inc. (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed by the registrant on May 30, 2024). | |
| 3.3 | Certificate of Amendment to the Fourth Amended and Restated Certificate of Incorporation of Clene Inc. (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed by the registrant on July 9, 2024). | |
| 3.4 |
Bylaws of Clene Inc. (incorporated by reference to Exhibit 3.2 to the Current Report on Form 8-K filed by the Registrant on January 5, 2021). |
|
| 10.1# | Equity Distribution Agreement, dated April 28, 2025, by and between Clene Inc. and Canaccord Genuity LLC (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed by the registrant on April 28, 2025). | |
| 10.2 | Clene Inc. Amended 2020 Stock Plan (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed by the registrant on May 23, 2025). | |
| 10.3 | Clene Inc. Amended Board of Directors Compensation Program (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed by the registrant on May 23, 2025). | |
| 31.1* |
Certification of Chief Executive Officer pursuant to Rule 13a-14(a) and Rule 15d-14(a), promulgated under the Securities and Exchange Act of 1934, as amended. |
|
| 31.2* |
Certification of Chief Financial Officer pursuant to Rule 13a-14(a) and Rule 15d-14(a), promulgated under the Securities and Exchange Act of 1934, as amended. |
|
| 32.1** |
Certification of Chief Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. |
|
| 32.2** |
Certification of Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. |
|
| 101.INS |
Inline XBRL Instance Document. |
|
| 101.SCH |
Inline XBRL Taxonomy Extension Schema Document. |
|
| 101.CAL |
Inline XBRL Taxonomy Extension Calculation Linkbase Document. |
|
| 101.DEF |
Inline XBRL Taxonomy Extension Definition Linkbase Document. |
|
| 101.LAB |
Inline XBRL Taxonomy Extension Label Linkbase Document. |
|
| 101.PRE |
Inline XBRL Taxonomy Extension Presentation Linkbase Document. |
|
| 104 |
Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101). |
| * |
Filed herewith. |
| ** |
Furnished herewith. |
| # | Schedules and similar attachments to this exhibit have been omitted pursuant to Item 601(a)(5) of Regulation S-K. We agree to furnish supplementally a copy of such omitted materials to the SEC upon request. |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
| CLENE INC. |
||
| Dated: August 14, 2025 |
By: |
/s/ Robert Etherington |
| Name: |
Robert Etherington |
|
| Title: |
President, Chief Executive Officer and Director |
|
| Dated: August 14, 2025 |
By: |
/s/ Morgan R. Brown |
| Name: |
Morgan R. Brown |
|
| Title: |
Chief Financial Officer |
|
Source:
