AG˹ٷ

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[Form 4] GCT Semiconductor Holding, Inc. Insider Trading Activity

Filing Impact
(Low)
Filing Sentiment
(Neutral)
Form Type
4
Rhea-AI Filing Summary

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) has filed a preliminary prospectus supplement under its effective shelf to raise capital through a combined offering of: (i) shares of common stock or pre-funded warrants (exercise price $0.001) in lieu of common stock, (ii) Series A warrants, and (iii) Series B warrants. Every share (or pre-funded warrant) will be sold together with one Series A warrant and one Series B warrant, although the securities are immediately separable upon issuance.

  • Pricing & size: Key economics—number of securities, combined public price, underwriting discount, and gross/net proceeds—remain blank pending final marketing, but the filing authorizes a 30-day overallotment option for additional shares and warrants.
  • Warrant profile: � Series A warrants are exercisable immediately, expire on the earlier of (a) 30 days after FDA accepts a Biologics License Application (BLA) for INO-3107 or (b) 12 months after issuance; � Series B warrants are exercisable immediately and expire five years after issuance. Neither series will be listed, limiting liquidity.
  • Use of proceeds: Management plans to direct funds to (1) advancement of its DNA-medicine clinical pipeline—including a rolling BLA submission for lead asset INO-3107 in recurrent respiratory papillomatosis expected to begin mid-2025, (2) potential commercial launch preparation for INO-3107 if approved, and (3) general corporate purposes.
  • Dilution & risk: The company warns that investors will incur immediate dilution; further dilution could arise from outstanding equity awards (�2.6 m shares), legacy warrants (�10 m at $3.76) and future ATM sales ($57.9 m capacity). Inovio remains a clinical-stage biotech with no product revenue, significant accumulated deficits, and multiple R&D, regulatory, manufacturing and financing risks.
  • Corporate status: Inovio is a “smaller reporting company,� enabling reduced SEC disclosure. Piper Sandler is sole book-running manager.

Because amounts are placeholders, the filing primarily signals intent to strengthen the balance sheet ahead of key regulatory catalysts rather than conveying finalized financial impact.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) ha presentato un supplemento preliminare al prospetto nell'ambito del suo shelf efficace per raccogliere capitale tramite un'offerta combinata di: (i) azioni ordinarie o warrant pre-finanziati (prezzo di esercizio $0,001) in sostituzione delle azioni ordinarie, (ii) warrant di Serie A e (iii) warrant di Serie B. Ogni azione (o warrant pre-finanziato) sarà venduta insieme a un warrant di Serie A e un warrant di Serie B, sebbene i titoli siano immediatamente separabili al momento dell'emissione.

  • Prezzi e dimensioni: Le condizioni chiave � numero di titoli, prezzo pubblico combinato, sconto di sottoscrizione e proventi lordi/netti � sono al momento non specificate in attesa del marketing finale, ma il deposito autorizza un'opzione di sovrallocazione di 30 giorni per azioni e warrant aggiuntivi.
  • Profilo dei warrant: � I warrant di Serie A sono esercitabili immediatamente e scadono al primo tra (a) 30 giorni dopo l'accettazione da parte della FDA di una Biologics License Application (BLA) per INO-3107 o (b) 12 mesi dall'emissione; � i warrant di Serie B sono esercitabili immediatamente e scadono cinque anni dopo l'emissione. Nessuna delle due serie sarà quotata, limitando la liquidità.
  • Utilizzo dei proventi: La direzione intende destinare i fondi a (1) avanzamento della pipeline clinica di medicina del DNA � incluso l'invio progressivo della BLA per il principale asset INO-3107 nella papillomatosi respiratoria ricorrente, previsto per metà 2025, (2) preparativi per un potenziale lancio commerciale di INO-3107 in caso di approvazione e (3) scopi aziendali generali.
  • Diluizione e rischi: La società avverte che gli investitori subiranno una diluizione immediata; ulteriori diluizioni potrebbero derivare da premi azionari in essere (circa 2,6 milioni di azioni), warrant legacy (circa 10 milioni a $3,76) e future vendite ATM (capacità di $57,9 milioni). Inovio è ancora una biotech in fase clinica senza ricavi da prodotti, con significativi deficit accumulati e molteplici rischi legati a R&S, regolamentazione, produzione e finanziamento.
  • Stato aziendale: Inovio è una “smaller reporting company�, che consente una riduzione delle divulgazioni SEC. Piper Sandler è l'unico gestore del libro ordini.

Poiché gli importi sono indicativi, il deposito segnala principalmente l'intenzione di rafforzare il bilancio in vista di importanti catalizzatori regolatori piuttosto che fornire un impatto finanziario definitivo.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) ha presentado un suplemento preliminar al prospecto bajo su programa de oferta efectiva para recaudar capital mediante una oferta combinada de: (i) acciones comunes o warrants prefinanciados (precio de ejercicio $0.001) en lugar de acciones comunes, (ii) warrants Serie A y (iii) warrants Serie B. Cada acción (o warrant prefinanciado) se venderá junto con un warrant Serie A y un warrant Serie B, aunque los valores son separables inmediatamente tras la emisión.

  • Precio y tamaño: Los términos clave � número de valores, precio público combinado, descuento de suscripción y productos brutos/netos � están pendientes y no se han especificado, pero la presentación autoriza una opción de sobresuscripción de 30 días para acciones y warrants adicionales.
  • Perfil de los warrants: � Los warrants Serie A son ejercitables inmediatamente y expiran al primero de (a) 30 días después de que la FDA acepte una Solicitud de Licencia Biológica (BLA) para INO-3107 o (b) 12 meses después de la emisión; � los warrants Serie B son ejercitables inmediatamente y expiran cinco años después de la emisión. Ninguna serie será listada, lo que limita la liquidez.
  • Uso de los ingresos: La dirección planea destinar los fondos a (1) avance de su pipeline clínico de medicina genética � incluyendo una presentación progresiva de la BLA para el principal activo INO-3107 en papilomatosis respiratoria recurrente prevista para mediados de 2025, (2) preparación para un posible lanzamiento comercial de INO-3107 si es aprobado, y (3) propósitos corporativos generales.
  • Dilución y riesgos: La compañía advierte que los inversores sufrirán dilución inmediata; diluciones adicionales podrían surgir de premios de capital pendientes (�2.6 millones de acciones), warrants heredados (�10 millones a $3.76) y futuras ventas ATM (capacidad de $57.9 millones). Inovio sigue siendo una biotecnológica en etapa clínica sin ingresos por productos, con déficits acumulados significativos y múltiples riesgos en I+D, regulación, manufactura y financiamiento.
  • Estado corporativo: Inovio es una “smaller reporting company�, lo que permite una divulgación reducida ante la SEC. Piper Sandler es el único administrador del libro de órdenes.

Dado que las cantidades son provisionales, la presentación señala principalmente la intención de fortalecer el balance antes de importantes catalizadores regulatorios en lugar de comunicar un impacto financiero finalizado.

Inovio Pharmaceuticals, Inc. (나스�: INO)� 유효� 셸프 등록� 통해 다음� 결합 공모� 통한 자본 조달� 목적으로 예비 증권 설명� 보충서를 제출했습니다: (i) 보통� 또는 보통� 대� 행사 가격이 $0.001� 선행행사 워런�, (ii) 시리� A 워런�, (iii) 시리� B 워런�. � 주식(또는 선행행사 워런�)은 하나� 시리� A 워런� � 하나� 시리� B 워런트와 함께 판매되며, 발행 즉시 증권은 분리 가능합니다.

  • 가� � 규모: 핵심 경제 조건—증� �, 결합 공모 가�, 인수 수수�, �/� 수익—은 최종 마케� 전까지 미정이며, 제출서류� 추가 주식 � 워런트에 대� 30일간� 초과배정 옵션� 허용합니�.
  • 워런� 프로�: � 시리� A 워런트는 즉시 행사 가능하�, INO-3107� 생물의약� 허가 신청�(BLA)가 FDA� 접수� � 30� 또는 발행 � 12개월 � 빠른 시점� 만료됩니�; � 시리� B 워런트는 즉시 행사 가능하� 발행 � 5� 만료됩니�. � 시리� 모두 상장되지 않아 유동성이 제한됩니�.
  • 수익� 사용: 경영진은 자금� (1) DNA 의약� 임상 파이프라� 진전—재발성 호흡� 유두종증 치료� INO-3107� 롤링 BLA 제출� 2025� 중반 시작 예정, (2) 승인 � INO-3107 상업� 출시 준�, (3) 일반 기업 목적� 사용� 계획입니�.
  • 희석 � 위험: 회사� 투자자들� 즉각적인 희석� 경험� 것이라고 경고하며, 추가 희석은 미지� 주식 보상(� 260� �), 기존 워런�(� 1000� �, 행사 가� $3.76), 향후 ATM 판매(� $5790� 규모)� 인해 발생� � 있습니다. 이노비오� 제품 매출� 없는 임상 단계 바이오텍으로, 누적 적자가 크고 연구개발, 규제, 제조 � 자금 조달 관� 위험� 다수 존재합니�.
  • 기업 현황: 이노비오� SEC 공시가 간소화되� “소규모 보고 회사”이�, Piper Sandler가 단독 주관사로 참여합니�.

금액� 잠정적이므� 이번 제출은 주요 규제 촉매 � 재무구조 강화 의도� 주로 나타내며, 확정� 재무 영향은 아닙니다.

Inovio Pharmaceuticals, Inc. (Nasdaq : INO) a déposé un supplément préliminaire au prospectus dans le cadre de son programme d’enregistrement effectif afin de lever des fonds via une offre combinée comprenant : (i) des actions ordinaires ou des bons de souscription préfinancés (prix d’exercice de 0,001 $) en lieu et place des actions ordinaires, (ii) des bons de souscription de Série A, et (iii) des bons de souscription de Série B. Chaque action (ou bon préfinancé) sera vendue avec un bon de souscription de Série A et un bon de souscription de Série B, bien que les titres soient immédiatement dissociables à l’émission.

  • Tarification et taille : Les paramètres clés � nombre de titres, prix public combiné, décote de souscription, et produit brut/net � restent à définir en attente du marketing final, mais le dépôt autorise une option de surallocation de 30 jours pour des actions et bons supplémentaires.
  • Profil des bons de souscription : � Les bons de Série A sont exerçables immédiatement et expirent au plus tôt entre (a) 30 jours après l’acceptation par la FDA d’une demande d’autorisation de mise sur le marché biologique (BLA) pour INO-3107, ou (b) 12 mois après émission ; � les bons de Série B sont exerçables immédiatement et expirent cinq ans après émission. Aucune série ne sera cotée, limitant la liquidité.
  • Utilisation des fonds : La direction prévoit d’allouer les fonds à (1) l’avancement de sa pipeline clinique de médecine à base d’ADN � y compris une soumission progressive de la BLA pour l’actif principal INO-3107 dans la papillomatose respiratoire récurrente prévue pour mi-2025, (2) la préparation d’un lancement commercial potentiel de INO-3107 en cas d’approbation, et (3) des fins générales d’entreprise.
  • Dilution et risques : La société avertit que les investisseurs subiront une dilution immédiate ; une dilution supplémentaire pourrait provenir des attributions d’actions en cours (�2,6 millions d’actions), des bons historiques (�10 millions à 3,76 $) et des futures ventes ATM (capacité de 57,9 millions de dollars). Inovio reste une biotech en phase clinique sans revenus produits, avec des déficits accumulés importants et de multiples risques liés à la R&D, la réglementation, la fabrication et le financement.
  • Statut de la société : Inovio est une « smaller reporting company », ce qui permet une divulgation réduite auprès de la SEC. Piper Sandler est le seul gestionnaire principal.

Étant donné que les montants sont indicatifs, le dépôt signale principalement l’intention de renforcer le bilan avant des catalyseurs réglementaires clés plutôt que de fournir un impact financier finalisé.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) hat einen vorläufigen Nachtrag zum wirksamen Wertpapierprospekt eingereicht, um Kapital durch ein kombiniertes Angebot zu beschaffen, das umfasst: (i) Stammaktien oder vorausfinanzierte Optionsscheine (Ausübungspreis $0,001) anstelle von Stammaktien, (ii) Serie A Optionsscheine und (iii) Serie B Optionsscheine. Jede Aktie (oder vorausfinanzierter Optionsschein) wird zusammen mit einem Optionsschein der Serie A und einem der Serie B verkauft, wobei die Wertpapiere sofort nach Ausgabe trennbar sind.

  • Preisgestaltung & Größe: Wichtige wirtschaftliche Eckdaten � Anzahl der Wertpapiere, kombinierter öffentlicher Preis, Underwriting-Rabatt sowie Brutto-/Nettoprovisionen � sind noch offen und werden nach Abschluss des Marketings festgelegt. Die Einreichung erlaubt eine 30-tägige Überzuteilungsoption für zusätzliche Aktien und Optionsscheine.
  • Optionsscheinprofil: � Serie A Optionsscheine sind sofort ausübbar und verfallen am früheren Zeitpunkt von (a) 30 Tagen nach FDA-Akzeptanz eines Biologics License Application (BLA) für INO-3107 oder (b) 12 Monaten nach Ausgabe; � Serie B Optionsscheine sind sofort ausübbar und verfallen fünf Jahre nach Ausgabe. Keine der Serien wird gelistet, was die Liquidität einschränkt.
  • Verwendung der Erlöse: Das Management plant die Mittel für (1) den Fortschritt der DNA-Medizin-Produktpipeline � einschließlich einer rollierenden BLA-Einreichung für den Hauptwirkstoff INO-3107 bei rezidivierender respiratorischer Papillomatose, die Mitte 2025 beginnen soll, (2) potenzielle kommerzielle Markteinführungsvorbereitungen für INO-3107 bei Zulassung und (3) allgemeine Unternehmenszwecke zu verwenden.
  • Verwässerung & Risiko: Das Unternehmen warnt, dass Investoren eine sofortige Verwässerung erleiden; weitere Verwässerungen könnten durch ausstehende Aktienprämien (ca. 2,6 Mio. Aktien), Alt-Optionsscheine (ca. 10 Mio. zu $3,76) und künftige ATM-Verkäufe (Kapazität $57,9 Mio.) entstehen. Inovio ist weiterhin ein Biotech-Unternehmen in der klinischen Phase ohne Produktumsatz, mit erheblichen kumulierten Verlusten und vielfältigen Risiken in F&E, Regulierung, Herstellung und Finanzierung.
  • Unternehmensstatus: Inovio ist ein „smaller reporting company�, was reduzierte SEC-Offenlegung ermöglicht. Piper Sandler ist alleiniger Bookrunner.

Da die Beträge Platzhalter sind, signalisiert die Einreichung vor allem die Absicht, die Bilanz vor wichtigen regulatorischen Ereignissen zu stärken, anstatt endgültige finanzielle Auswirkungen darzustellen.

Positive
  • Capital access: Offering should provide fresh cash to fund INO-3107 BLA submission, confirmatory trial and eventual commercial launch preparation.
  • Regulatory momentum: FDA has indicated completed data support an accelerated-approval BLA; manufacturing issue with CELLECTRA 5PSP has been resolved, enabling mid-2025 rolling submission timeline.
  • Pipeline breadth: Additional candidates (INO-3112, INO-5401) and multiple partnerships (e.g., Coherus, AstraZeneca) offer diversified optionality beyond INO-3107.
Negative
  • Dilution risk: New equity plus two layers of investor warrants will increase share count; exact magnitude TBD once pricing is finalized.
  • Liquidity limits: Warrants will not be exchange-listed, potentially reducing attractiveness and aftermarket price discovery.
  • No revenue base: Company remains pre-commercial with continued operating losses; success hinges on regulatory approvals and further financing.
  • Unspecified terms: Blank placeholders for size, price and proceeds create valuation uncertainty for existing and prospective shareholders.

Insights

TL;DR Capital raise readies Inovio for INO-3107 BLA costs but adds dilution; warrant structure tightens near-term cash while preserving future optionality.

Funding rationale: Inovio’s cash burn will accelerate as it scales manufacturing, device validation and a confirmatory Phase 3 trial for INO-3107. The offering—despite undisclosed size—should extend runway beyond the anticipated FDA file-acceptance target (YE-2025) and reduce financing overhang.
Structural observations: Coupling shares/pre-funded warrants with two warrant tranches provides investors leverage but caps near-term dilution (Series A’s short life) while offering longer-dated upside (Series B). The unusual trigger for Series A expiry�30 days post-BLA acceptance—aligns investor incentives with a key catalyst.
Valuation impact: Lack of concrete pricing keeps the raise’s EPS effect indeterminate; however, even a mid-single-digit million share issuance would be material given only ~36.7 m shares outstanding. Non-listing of warrants could dampen demand from certain funds.
Risk skew: Still no approved products; any device or clinical setback could stall the BLA, nullifying Series A warrant value and pressuring the stock. Overall, transaction impact leans neutral until final terms emerge.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) ha presentato un supplemento preliminare al prospetto nell'ambito del suo shelf efficace per raccogliere capitale tramite un'offerta combinata di: (i) azioni ordinarie o warrant pre-finanziati (prezzo di esercizio $0,001) in sostituzione delle azioni ordinarie, (ii) warrant di Serie A e (iii) warrant di Serie B. Ogni azione (o warrant pre-finanziato) sarà venduta insieme a un warrant di Serie A e un warrant di Serie B, sebbene i titoli siano immediatamente separabili al momento dell'emissione.

  • Prezzi e dimensioni: Le condizioni chiave � numero di titoli, prezzo pubblico combinato, sconto di sottoscrizione e proventi lordi/netti � sono al momento non specificate in attesa del marketing finale, ma il deposito autorizza un'opzione di sovrallocazione di 30 giorni per azioni e warrant aggiuntivi.
  • Profilo dei warrant: � I warrant di Serie A sono esercitabili immediatamente e scadono al primo tra (a) 30 giorni dopo l'accettazione da parte della FDA di una Biologics License Application (BLA) per INO-3107 o (b) 12 mesi dall'emissione; � i warrant di Serie B sono esercitabili immediatamente e scadono cinque anni dopo l'emissione. Nessuna delle due serie sarà quotata, limitando la liquidità.
  • Utilizzo dei proventi: La direzione intende destinare i fondi a (1) avanzamento della pipeline clinica di medicina del DNA � incluso l'invio progressivo della BLA per il principale asset INO-3107 nella papillomatosi respiratoria ricorrente, previsto per metà 2025, (2) preparativi per un potenziale lancio commerciale di INO-3107 in caso di approvazione e (3) scopi aziendali generali.
  • Diluizione e rischi: La società avverte che gli investitori subiranno una diluizione immediata; ulteriori diluizioni potrebbero derivare da premi azionari in essere (circa 2,6 milioni di azioni), warrant legacy (circa 10 milioni a $3,76) e future vendite ATM (capacità di $57,9 milioni). Inovio è ancora una biotech in fase clinica senza ricavi da prodotti, con significativi deficit accumulati e molteplici rischi legati a R&S, regolamentazione, produzione e finanziamento.
  • Stato aziendale: Inovio è una “smaller reporting company�, che consente una riduzione delle divulgazioni SEC. Piper Sandler è l'unico gestore del libro ordini.

Poiché gli importi sono indicativi, il deposito segnala principalmente l'intenzione di rafforzare il bilancio in vista di importanti catalizzatori regolatori piuttosto che fornire un impatto finanziario definitivo.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) ha presentado un suplemento preliminar al prospecto bajo su programa de oferta efectiva para recaudar capital mediante una oferta combinada de: (i) acciones comunes o warrants prefinanciados (precio de ejercicio $0.001) en lugar de acciones comunes, (ii) warrants Serie A y (iii) warrants Serie B. Cada acción (o warrant prefinanciado) se venderá junto con un warrant Serie A y un warrant Serie B, aunque los valores son separables inmediatamente tras la emisión.

  • Precio y tamaño: Los términos clave � número de valores, precio público combinado, descuento de suscripción y productos brutos/netos � están pendientes y no se han especificado, pero la presentación autoriza una opción de sobresuscripción de 30 días para acciones y warrants adicionales.
  • Perfil de los warrants: � Los warrants Serie A son ejercitables inmediatamente y expiran al primero de (a) 30 días después de que la FDA acepte una Solicitud de Licencia Biológica (BLA) para INO-3107 o (b) 12 meses después de la emisión; � los warrants Serie B son ejercitables inmediatamente y expiran cinco años después de la emisión. Ninguna serie será listada, lo que limita la liquidez.
  • Uso de los ingresos: La dirección planea destinar los fondos a (1) avance de su pipeline clínico de medicina genética � incluyendo una presentación progresiva de la BLA para el principal activo INO-3107 en papilomatosis respiratoria recurrente prevista para mediados de 2025, (2) preparación para un posible lanzamiento comercial de INO-3107 si es aprobado, y (3) propósitos corporativos generales.
  • Dilución y riesgos: La compañía advierte que los inversores sufrirán dilución inmediata; diluciones adicionales podrían surgir de premios de capital pendientes (�2.6 millones de acciones), warrants heredados (�10 millones a $3.76) y futuras ventas ATM (capacidad de $57.9 millones). Inovio sigue siendo una biotecnológica en etapa clínica sin ingresos por productos, con déficits acumulados significativos y múltiples riesgos en I+D, regulación, manufactura y financiamiento.
  • Estado corporativo: Inovio es una “smaller reporting company�, lo que permite una divulgación reducida ante la SEC. Piper Sandler es el único administrador del libro de órdenes.

Dado que las cantidades son provisionales, la presentación señala principalmente la intención de fortalecer el balance antes de importantes catalizadores regulatorios en lugar de comunicar un impacto financiero finalizado.

Inovio Pharmaceuticals, Inc. (나스�: INO)� 유효� 셸프 등록� 통해 다음� 결합 공모� 통한 자본 조달� 목적으로 예비 증권 설명� 보충서를 제출했습니다: (i) 보통� 또는 보통� 대� 행사 가격이 $0.001� 선행행사 워런�, (ii) 시리� A 워런�, (iii) 시리� B 워런�. � 주식(또는 선행행사 워런�)은 하나� 시리� A 워런� � 하나� 시리� B 워런트와 함께 판매되며, 발행 즉시 증권은 분리 가능합니다.

  • 가� � 규모: 핵심 경제 조건—증� �, 결합 공모 가�, 인수 수수�, �/� 수익—은 최종 마케� 전까지 미정이며, 제출서류� 추가 주식 � 워런트에 대� 30일간� 초과배정 옵션� 허용합니�.
  • 워런� 프로�: � 시리� A 워런트는 즉시 행사 가능하�, INO-3107� 생물의약� 허가 신청�(BLA)가 FDA� 접수� � 30� 또는 발행 � 12개월 � 빠른 시점� 만료됩니�; � 시리� B 워런트는 즉시 행사 가능하� 발행 � 5� 만료됩니�. � 시리� 모두 상장되지 않아 유동성이 제한됩니�.
  • 수익� 사용: 경영진은 자금� (1) DNA 의약� 임상 파이프라� 진전—재발성 호흡� 유두종증 치료� INO-3107� 롤링 BLA 제출� 2025� 중반 시작 예정, (2) 승인 � INO-3107 상업� 출시 준�, (3) 일반 기업 목적� 사용� 계획입니�.
  • 희석 � 위험: 회사� 투자자들� 즉각적인 희석� 경험� 것이라고 경고하며, 추가 희석은 미지� 주식 보상(� 260� �), 기존 워런�(� 1000� �, 행사 가� $3.76), 향후 ATM 판매(� $5790� 규모)� 인해 발생� � 있습니다. 이노비오� 제품 매출� 없는 임상 단계 바이오텍으로, 누적 적자가 크고 연구개발, 규제, 제조 � 자금 조달 관� 위험� 다수 존재합니�.
  • 기업 현황: 이노비오� SEC 공시가 간소화되� “소규모 보고 회사”이�, Piper Sandler가 단독 주관사로 참여합니�.

금액� 잠정적이므� 이번 제출은 주요 규제 촉매 � 재무구조 강화 의도� 주로 나타내며, 확정� 재무 영향은 아닙니다.

Inovio Pharmaceuticals, Inc. (Nasdaq : INO) a déposé un supplément préliminaire au prospectus dans le cadre de son programme d’enregistrement effectif afin de lever des fonds via une offre combinée comprenant : (i) des actions ordinaires ou des bons de souscription préfinancés (prix d’exercice de 0,001 $) en lieu et place des actions ordinaires, (ii) des bons de souscription de Série A, et (iii) des bons de souscription de Série B. Chaque action (ou bon préfinancé) sera vendue avec un bon de souscription de Série A et un bon de souscription de Série B, bien que les titres soient immédiatement dissociables à l’émission.

  • Tarification et taille : Les paramètres clés � nombre de titres, prix public combiné, décote de souscription, et produit brut/net � restent à définir en attente du marketing final, mais le dépôt autorise une option de surallocation de 30 jours pour des actions et bons supplémentaires.
  • Profil des bons de souscription : � Les bons de Série A sont exerçables immédiatement et expirent au plus tôt entre (a) 30 jours après l’acceptation par la FDA d’une demande d’autorisation de mise sur le marché biologique (BLA) pour INO-3107, ou (b) 12 mois après émission ; � les bons de Série B sont exerçables immédiatement et expirent cinq ans après émission. Aucune série ne sera cotée, limitant la liquidité.
  • Utilisation des fonds : La direction prévoit d’allouer les fonds à (1) l’avancement de sa pipeline clinique de médecine à base d’ADN � y compris une soumission progressive de la BLA pour l’actif principal INO-3107 dans la papillomatose respiratoire récurrente prévue pour mi-2025, (2) la préparation d’un lancement commercial potentiel de INO-3107 en cas d’approbation, et (3) des fins générales d’entreprise.
  • Dilution et risques : La société avertit que les investisseurs subiront une dilution immédiate ; une dilution supplémentaire pourrait provenir des attributions d’actions en cours (�2,6 millions d’actions), des bons historiques (�10 millions à 3,76 $) et des futures ventes ATM (capacité de 57,9 millions de dollars). Inovio reste une biotech en phase clinique sans revenus produits, avec des déficits accumulés importants et de multiples risques liés à la R&D, la réglementation, la fabrication et le financement.
  • Statut de la société : Inovio est une « smaller reporting company », ce qui permet une divulgation réduite auprès de la SEC. Piper Sandler est le seul gestionnaire principal.

Étant donné que les montants sont indicatifs, le dépôt signale principalement l’intention de renforcer le bilan avant des catalyseurs réglementaires clés plutôt que de fournir un impact financier finalisé.

Inovio Pharmaceuticals, Inc. (Nasdaq: INO) hat einen vorläufigen Nachtrag zum wirksamen Wertpapierprospekt eingereicht, um Kapital durch ein kombiniertes Angebot zu beschaffen, das umfasst: (i) Stammaktien oder vorausfinanzierte Optionsscheine (Ausübungspreis $0,001) anstelle von Stammaktien, (ii) Serie A Optionsscheine und (iii) Serie B Optionsscheine. Jede Aktie (oder vorausfinanzierter Optionsschein) wird zusammen mit einem Optionsschein der Serie A und einem der Serie B verkauft, wobei die Wertpapiere sofort nach Ausgabe trennbar sind.

  • Preisgestaltung & Größe: Wichtige wirtschaftliche Eckdaten � Anzahl der Wertpapiere, kombinierter öffentlicher Preis, Underwriting-Rabatt sowie Brutto-/Nettoprovisionen � sind noch offen und werden nach Abschluss des Marketings festgelegt. Die Einreichung erlaubt eine 30-tägige Überzuteilungsoption für zusätzliche Aktien und Optionsscheine.
  • Optionsscheinprofil: � Serie A Optionsscheine sind sofort ausübbar und verfallen am früheren Zeitpunkt von (a) 30 Tagen nach FDA-Akzeptanz eines Biologics License Application (BLA) für INO-3107 oder (b) 12 Monaten nach Ausgabe; � Serie B Optionsscheine sind sofort ausübbar und verfallen fünf Jahre nach Ausgabe. Keine der Serien wird gelistet, was die Liquidität einschränkt.
  • Verwendung der Erlöse: Das Management plant die Mittel für (1) den Fortschritt der DNA-Medizin-Produktpipeline � einschließlich einer rollierenden BLA-Einreichung für den Hauptwirkstoff INO-3107 bei rezidivierender respiratorischer Papillomatose, die Mitte 2025 beginnen soll, (2) potenzielle kommerzielle Markteinführungsvorbereitungen für INO-3107 bei Zulassung und (3) allgemeine Unternehmenszwecke zu verwenden.
  • Verwässerung & Risiko: Das Unternehmen warnt, dass Investoren eine sofortige Verwässerung erleiden; weitere Verwässerungen könnten durch ausstehende Aktienprämien (ca. 2,6 Mio. Aktien), Alt-Optionsscheine (ca. 10 Mio. zu $3,76) und künftige ATM-Verkäufe (Kapazität $57,9 Mio.) entstehen. Inovio ist weiterhin ein Biotech-Unternehmen in der klinischen Phase ohne Produktumsatz, mit erheblichen kumulierten Verlusten und vielfältigen Risiken in F&E, Regulierung, Herstellung und Finanzierung.
  • Unternehmensstatus: Inovio ist ein „smaller reporting company�, was reduzierte SEC-Offenlegung ermöglicht. Piper Sandler ist alleiniger Bookrunner.

Da die Beträge Platzhalter sind, signalisiert die Einreichung vor allem die Absicht, die Bilanz vor wichtigen regulatorischen Ereignissen zu stärken, anstatt endgültige finanzielle Auswirkungen darzustellen.

SEC Form 4
FORM 4 UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

STATEMENT OF CHANGES IN BENEFICIAL OWNERSHIP

Filed pursuant to Section 16(a) of the Securities Exchange Act of 1934
or Section 30(h) of the Investment Company Act of 1940
OMB APPROVAL
OMB Number: 3235-0287
Estimated average burden
hours per response: 0.5
Check this box if no longer subject to Section 16. Form 4 or Form 5 obligations may continue. See Instruction 1(b).
Check this box to indicate that a transaction was made pursuant to a contract, instruction or written plan for the purchase or sale of equity securities of the issuer that is intended to satisfy the affirmative defense conditions of Rule 10b5-1(c). See Instruction 10.
1. Name and Address of Reporting Person*
Barker Robert

(Last) (First) (Middle)
C/O GCT SEMICONDUCTOR HOLDING, INC.
2290 NORTH 1ST STREET, SUITE 201

(Street)
SAN JOSE CA 95131

(City) (State) (Zip)
2. Issuer Name and Ticker or Trading Symbol
GCT Semiconductor Holding, Inc. [ GCTS ]
5. Relationship of Reporting Person(s) to Issuer
(Check all applicable)
X Director 10% Owner
Officer (give title below) X Other (specify below)
Class II Director
3. Date of Earliest Transaction (Month/Day/Year)
06/30/2025
4. If Amendment, Date of Original Filed (Month/Day/Year)
6. Individual or Joint/Group Filing (Check Applicable Line)
X Form filed by One Reporting Person
Form filed by More than One Reporting Person
Table I - Non-Derivative Securities Acquired, Disposed of, or Beneficially Owned
1. Title of Security (Instr. 3) 2. Transaction Date (Month/Day/Year) 2A. Deemed Execution Date, if any (Month/Day/Year) 3. Transaction Code (Instr. 8) 4. Securities Acquired (A) or Disposed Of (D) (Instr. 3, 4 and 5) 5. Amount of Securities Beneficially Owned Following Reported Transaction(s) (Instr. 3 and 4) 6. Ownership Form: Direct (D) or Indirect (I) (Instr. 4) 7. Nature of Indirect Beneficial Ownership (Instr. 4)
Code V Amount (A) or (D) Price
Common Stock 06/30/2025 A 18,456(1)(2)(3)(4) A $0 77,321 D
Table II - Derivative Securities Acquired, Disposed of, or Beneficially Owned
(e.g., puts, calls, warrants, options, convertible securities)
1. Title of Derivative Security (Instr. 3) 2. Conversion or Exercise Price of Derivative Security 3. Transaction Date (Month/Day/Year) 3A. Deemed Execution Date, if any (Month/Day/Year) 4. Transaction Code (Instr. 8) 5. Number of Derivative Securities Acquired (A) or Disposed of (D) (Instr. 3, 4 and 5) 6. Date Exercisable and Expiration Date (Month/Day/Year) 7. Title and Amount of Securities Underlying Derivative Security (Instr. 3 and 4) 8. Price of Derivative Security (Instr. 5) 9. Number of derivative Securities Beneficially Owned Following Reported Transaction(s) (Instr. 4) 10. Ownership Form: Direct (D) or Indirect (I) (Instr. 4) 11. Nature of Indirect Beneficial Ownership (Instr. 4)
Code V (A) (D) Date Exercisable Expiration Date Title Amount or Number of Shares
Explanation of Responses:
1. Each Restricted Stock Unit ("RSU") represents the right to receive one share of common stock, par value $0.0001 per share ("Common Stock") of GCT Semiconductor Holding, Inc. (the "Issuer") following vesting. The RSUs become payable in Common Stock in accordance with a deferral election made by the reporting person.
2. The number of shares subject to and issuable under the award is determined on the last day of each calendar quarter during the period April 1, 2025 through March 31, 2026 (beginning with the quarter ending June 30, 2025) by dividing $27,500 by the fair market value per share of Common Stock, which was determined to be $1.49 on June 30, 2025, rounded down to the nearest whole share.
3. The RSUs will vest on March 31, 2026, subject to continued service through such date.
4. No expiration date is applicable to restricted stock units.
/s/ Edmond Cheng, attorney-in-fact 07/01/2025
** Signature of Reporting Person Date
Reminder: Report on a separate line for each class of securities beneficially owned directly or indirectly.
* If the form is filed by more than one reporting person, see Instruction 4 (b)(v).
** Intentional misstatements or omissions of facts constitute Federal Criminal Violations See 18 U.S.C. 1001 and 15 U.S.C. 78ff(a).
Note: File three copies of this Form, one of which must be manually signed. If space is insufficient, see Instruction 6 for procedure.
Persons who respond to the collection of information contained in this form are not required to respond unless the form displays a currently valid OMB Number.

FAQ

What is Inovio Pharmaceuticals (INO) selling in this 424B5 offering?

INO is offering shares of common stock—or pre-funded warrants in lieu of shares—bundled with Series A and Series B common-stock warrants. All securities are immediately separable but must be purchased together.

Why is Inovio raising capital now?

Proceeds will support continued development of its DNA-medicine pipeline, notably the rolling BLA submission and potential commercial launch of lead candidate INO-3107, plus general corporate purposes.

How long do the new warrants last?

Series A warrants expire on the earlier of 30 days after FDA accepts the INO-3107 BLA or 12 months post-issuance; Series B warrants expire five years after issuance.

Will the pre-funded and common stock warrants trade on Nasdaq?

No. Inovio does not intend to list the pre-funded, Series A or Series B warrants on any securities exchange, so liquidity will be limited.

What dilution should current INO shareholders expect?

Exact impact is unknown until pricing is set, but any issuance adds to ~36.7 m shares outstanding and sits on top of ~12.9 m potential shares from existing options and warrants.

How is Inovio addressing past device manufacturing issues?

The company states it resolved a manufacturing issue with the single-use component of its CELLECTRA 5PSP device in Q1-2025, clearing the path for a confirmatory trial and BLA filing.
GCT Semiconductor Holding, Inc.

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Semiconductors
Semiconductors & Related Devices
United States
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