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Annovis Provides Corporate Updates and Reports Second Quarter 2025 Financial Results

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Annovis Bio (NYSE: ANVS), a late-stage clinical drug platform company focused on neurodegenerative diseases, provided Q2 2025 updates on its clinical progress and financial results. The company's pivotal Phase 3 trial for early Alzheimer's disease has secured 76 U.S. clinical sites, with 38 patients already receiving treatment and approximately 200 more in screening.

Key operational highlights include the appointment of Hui Liu as Director of Biostatistics, successful presentations at AAIC 2025, and the completion of patent family transfers to crystal buntanetap. Financially, Annovis reported cash and equivalents of $17.1 million as of June 30, 2025, with reduced R&D expenses of $5.2 million and G&A expenses of $1.1 million for Q2 2025. The company's net loss per share improved to $0.32 compared to $0.44 in the same quarter last year.

Annovis Bio (NYSE: ANVS), azienda farmaceutica in fase clinica avanzata specializzata nelle malattie neurodegenerative, ha fornito aggiornamenti del secondo trimestre 2025 sul progresso clinico e sui risultati finanziari. Il trial di Fase 3 cruciale per l'Alzheimer in fase iniziale ha coinvolto 76 siti clinici negli Stati Uniti, con 38 pazienti già in trattamento e circa 200 ulteriori in fase di screening.

I principali elementi operativi includono la nomina di Hui Liu a Direttore della Biostatistica, presentazioni di successo all'AAIC 2025 e il completamento del trasferimento delle famiglie di brevetti a crystal buntanetap. Sul piano finanziario, Annovis ha dichiarato liquidità e mezzi equivalenti di $17.1 million al 30 giugno 2025, con costi di R&S ridotti a $5.2 million e spese G&A pari a $1.1 million per il secondo trimestre 2025. Il risultato netto per azione è migliorato a $0.32 rispetto a $0.44 nello stesso periodo dell'anno precedente.

Annovis Bio (NYSE: ANVS), una compañía farmacéutica en fase clínica avanzada centrada en enfermedades neurodegenerativas, presentó actualizaciones del segundo trimestre de 2025 sobre su avance clínico y sus resultados financieros. El ensayo pivotal de Fase 3 para la enfermedad de Alzheimer en etapa temprana cuenta con 76 sitios clínicos en EE. UU., con 38 pacientes ya recibiendo tratamiento y aproximadamente 200 más en cribado.

Los aspectos operativos clave incluyen el nombramiento de Hui Liu como Directora de Bioestadística, presentaciones exitosas en AAIC 2025 y la finalización de las transferencias de familias de patentes a crystal buntanetap. En lo financiero, Annovis informó de efectivo y equivalentes por $17.1 million al 30 de junio de 2025, con gastos de I+D reducidos a $5.2 million y gastos G&A de $1.1 million en el segundo trimestre de 2025. La pérdida neta por acción mejoró a $0.32 frente a $0.44 en el mismo trimestre del año anterior.

Annovis Bio (NYSE: ANVS)� 신경퇴행� 질환� 주력하는 후기 임상 단계� 신약 플랫� 기업으로� 2025� 2분기 임상 진행 상황 � 재무 결과� 업데이트했습니다. 회사� 초기 알츠하이머병� 대상으� � 핵심 3� 시험은 미국 � 76� 임상 사이트를 확보했으�, 이미 38명이 치료� 받고 있고 � 200명가량이 스크리닝 중입니다.

주요 운영 하이라이트로� Hui Liu� 생물통계� 이사 선임, AAIC 2025에서� 성공� 발표, 그리� 특허 군의 crystal buntanetap로의 이전 완료가 포함됩니�. 재무적으� Annovis� 2025� 6� 30� 기준 현금 � 현금� 자산 $17.1 million� 보고했으�, 2025� 2분기 연구개발비는 $5.2 million, 일반관리비� $1.1 million� 감소했습니다. 주당 순손실은 전년 동기 $0.44에서 개선� $0.32� 기록했습니다.

Annovis Bio (NYSE: ANVS), société de biotechnologie en phase clinique avancée spécialisée dans les maladies neurodégénératives, a publié des mises à jour du deuxième trimestre 2025 sur ses progrès cliniques et ses résultats financiers. L'essai pivot de Phase 3 pour la maladie d'Alzheimer précoce a mobilisé 76 sites cliniques aux États-Unis, avec 38 patients déjà traités et environ 200 autres en phase de sélection.

Les faits marquants opérationnels incluent la nomination de Hui Liu au poste de directrice de la biostatistique, des présentations réussies à l'AAIC 2025 et l'achèvement des transferts de familles de brevets vers crystal buntanetap. Sur le plan financier, Annovis a déclaré des liquidités et équivalents de $17.1 million au 30 juin 2025, avec des dépenses R&D réduites à $5.2 million et des frais G&A de $1.1 million pour le deuxième trimestre 2025. La perte nette par action s'est améliorée à $0.32 contre $0.44 au même trimestre de l'année précédente.

Annovis Bio (NYSE: ANVS), ein spätphasiges klinisches Pharmaunternehmen mit Fokus auf neurodegenerative Erkrankungen, gab Updates zum zweiten Quartal 2025 zu seinem klinischen Fortschritt und den Finanzergebnissen bekannt. Die entscheidende Phase-3-Studie für frühe Alzheimer-Erkrankung umfasst 76 klinische Standorte in den USA; 38 Patienten erhalten bereits die Behandlung und etwa 200 weitere befinden sich im Screening.

Zu den wichtigen operativen Punkten zählen die Ernennung von Hui Liu zur Direktorin der Biostatistik, erfolgreiche Präsentationen auf der AAIC 2025 und der Abschluss der Übertragung von Patentfamilien an crystal buntanetap. Finanzseitig meldete Annovis Barmittel und Zahlungsmitteläquivalente in Höhe von $17.1 million zum 30. Juni 2025, mit reduzierten F&E-Aufwendungen von $5.2 million und G&A-Aufwendungen von $1.1 million im zweiten Quartal 2025. Der Verlust je Aktie verbesserte sich auf $0.32 gegenüber $0.44 im gleichen Quartal des Vorjahres.

Positive
  • Clinical trial progress with 76 secured sites and 38 patients already receiving treatment
  • Cash position improved to $17.1 million from $10.6 million in December 2024
  • Reduced net loss per share to $0.32 from $0.44 year-over-year
  • Decreased operating expenses with R&D at $5.2M (vs $5.8M) and G&A at $1.1M (vs $2.0M)
Negative
  • 50% screen failure rate in clinical trials
  • Continued net losses indicate ongoing cash burn

Insights

Annovis shows progress in Phase 3 Alzheimer's trial with 76 sites secured, reduced expenses, and improved cash position despite ongoing R&D investments.

Annovis Bio's Q2 2025 update demonstrates meaningful progress in its Phase 3 Alzheimer's disease program, with 76 clinical sites secured and 46 actively enrolling patients. The company has already dosed 38 subjects with either buntanetap or placebo, while nearly 200 more participants are in the screening pipeline. The 50% screen failure rate aligns with expectations for neurodegenerative disease trials, suggesting appropriate patient selection protocols.

On the financial front, Annovis has strengthened its position with $17.1 million in cash as of June 30, 2025, a substantial 61.3% increase from the $10.6 million reported at the end of 2024. This improved cash runway supports continued clinical development without immediate financing concerns. The company has simultaneously reduced its quarterly burn rate, with R&D expenses decreasing to $5.2 million from $5.8 million year-over-year, and G&A expenses dropping significantly to $1.1 million from $2.0 million. This cost discipline has contributed to a narrower loss of $0.32 per share compared to $0.44 in Q2 2024.

The successful transfer of all patent families to crystal buntanetap represents a critical intellectual property milestone, potentially extending exclusivity protection and enhancing the commercial value proposition. This strategic move, combined with the company's expanding clinical footprint and robust scientific presence at AAIC 2025, demonstrates management's focus on building long-term value while executing on near-term clinical goals for their neurodegenerative disease platform.

MALVERN, Pa., Aug. 12, 2025 (GLOBE NEWSWIRE) -- Annovis Bio, Inc. (NYSE: ANVS) ("Annovis" or the “Company�), a late-stage clinical drug platform company pioneering transformative therapies for neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD), today provided corporate updates and second quarter 2025 financial results.

“In the past quarter, our efforts were centered on driving enrollment for the pivotal Phase 3 trial in early AD, which now includes 76 secured clinical sites across the U.S. and over 400 patients screened to date,� said Maria Maccecchini, Ph.D., President and CEO of Annovis. “At the same time, we reached other notable milestones, including presenting our latest scientific findings at AAIC 2025 with the largest attendance ever from Annovis team and strengthening our global intellectual property protection by completing the transfer of all patent families to crystal buntanetap. As we move forward, our focus stays firmly on completing enrollment as planned to produce strong and trustworthy results, while also advancing our Parkinson’s program, with more updates coming as we progress.�

Clinical highlights

  • Annovis� pivotal Phase 3 study in early AD () is advancing rapidly, with 76 U.S. sites secured and 46 currently enrolling patients. The remaining sites are expected to begin enrollment shortly.
  • The pivotal Phase 3 trial has attracted strong participation, with 38 patients already receiving buntanetap or placebo and nearly 200 more in screening � a number that continues to grow each day � with screen failure rate being as expected at 50%.

Business highlights

  • In April, Annovis welcomed Hui Liu as Director of Biostatistics, who is responsible for maintaining statistical integrity of the data generated by the Company’s clinical trials.
  • In June, Annovis hosted a webcast to provide updates on its Phase 3 trial, engaging directly with the audience through a live Q&A session. The recording is available in the on the Company’s website.
  • In July, senior members of Annovis attended AAIC 2025 in Toronto, presenting four scientific posters highlighting advancements in the Alzheimer’s Phase 3 study and the pharmacokinetic profile of its lead drug candidate, buntanetap. All posters are available in the on the Company’s website.
  • In August, Annovis announced the successful transfer of all patent families to crystal buntanetap, achieving comprehensive global IP coverage for both the original and new forms of the Company’s drug candidate.

Financial results

  • Annovis� cash and cash equivalents totaled $17.1 million as of June 30, 2025, compared to $10.6 million as of December 31, 2024. The Company had 19.5 million shares of common stock outstanding as of June 30, 2025.
  • Research and development expenses for the three months ending June 30, 2025, were $5.2 million compared to $5.8 million for the three months ending June 30, 2024.
  • General and administrative expenses for the three months ending June 30, 2025, were $1.1 million compared to $2.0 million for the three months ending June 30, 2024.
  • Annovis reported a $0.32 basic and diluted net loss per common share for the three months ending June 30, 2025, compared to a $0.44 basic and diluted net loss per common share for the three months ending June 30, 2024.

About Annovis
Headquartered in Malvern, Pennsylvania, Annovis is dedicated to addressing neurodegeneration in diseases such as AD and PD. The Company is committed to developing innovative therapies that improve patient outcomes and quality of life. For more information, visit and follow us on , , and .

Investor Alerts
Interested investors and shareholders are encouraged to sign up for press releases and industry updates by registering for email alerts at .

Forward-Looking Statements
This press release contains forward-looking statements under the Securities Act of 1933 and the Securities Exchange Act of 1934, as amended. Actual results may differ due to various risks and uncertainties, including those outlined in the Company’s SEC filings under “Risk Factors� in its Annual Report on Form 10-K and Quarterly Reports on Form 10-Q. The Company undertakes no obligation to update forward-looking statements except as required by law.

Contact Information:
Annovis Bio Inc.
101 Lindenwood Drive
Suite 225
Malvern, PA 19355

Investor Contact:
Alexander Morin, Ph.D.
Director, Strategic Communications
Annovis Bio

(Tables to follow)

ANNOVIS BIO, INC.
Balance Sheets
(Unaudited)
June 30,December31,
2025
2024
Assets
Current assets:
Cash and cash equivalents$17,130,286$10,551,916
Prepaid expenses and other current assets4,324,2853,373,717
Total assets$21,454,571$13,925,633
Liabilities and stockholders� equity
Current liabilities:
Accounts payable$974,311$2,305,974
Accrued expenses1,830,8131,575,013
Total current liabilities2,805,1243,880,987
Non-current liabilities:
Warrant liability319,000737,000
Total liabilities3,124,1244,617,987
Commitments and contingencies
Stockholders� equity:
Preferred stock - $0.0001 par value, 2,000,000 shares authorized and 0 shares issued and outstanding
Common stock - $0.0001 par value, 70,000,000 shares authorized, 19,486,231 and 14,141,521 shares issued and outstanding at June30,2025 and December31,2024, respectively1,9481,414
Additional paid-in capital164,935,088144,155,694
Accumulated deficit(146,606,589)(134,849,462)
Total stockholders� equity18,330,4479,307,646
Total liabilities and stockholders� equity$21,454,571$13,925,633


ANNOVIS BIO, INC.
Statements of Operations
(Unaudited)
Three Months EndedSix Months Ended
June 30,June30,
2025
2024
2025
2024
Operating expenses:
Research and development$5,161,921$5,785,217$10,173,438$12,307,308
General and administrative1,109,5321,977,4212,380,6963,265,137
Total operating expenses6,271,4537,762,63812,554,13415,572,445
Operating loss(6,271,453)(7,762,638)(12,554,134)(15,572,445)
Other income (expense):
Interest income191,39525,978379,00770,146
Other financing costs(1,346,060)(1,346,060)
Change in fair value of warrants(140,000)4,062,308418,00010,761,000
Total other income, net51,3952,742,226797,0079,485,086
Net loss$(6,220,058)$(5,020,412)$(11,757,127)$(6,087,359)
Net loss per share
Basic$(0.32)$(0.44)$(0.64)$(0.56)
Diluted$(0.32)$(0.44)$(0.64)$(1.52)
Weighted-average number of common shares used in computing net loss per share
Basic19,486,23111,307,75918,464,87710,966,412
Diluted19,486,23111,307,75918,464,87711,066,265

FAQ

What is the status of Annovis Bio's (ANVS) Phase 3 Alzheimer's trial in Q2 2025?

The Phase 3 trial has secured 76 U.S. clinical sites, with 38 patients receiving buntanetap or placebo and approximately 200 more in screening. The trial has a 50% screen failure rate, which is within expected range.

How much cash does Annovis Bio (ANVS) have as of Q2 2025?

Annovis Bio reported $17.1 million in cash and cash equivalents as of June 30, 2025, an increase from $10.6 million as of December 31, 2024.

What were Annovis Bio's (ANVS) Q2 2025 financial results?

The company reported R&D expenses of $5.2 million, G&A expenses of $1.1 million, and a net loss of $0.32 per share for Q2 2025.

What major business developments did Annovis Bio (ANVS) announce in Q2 2025?

Key developments included hiring Hui Liu as Director of Biostatistics, presenting four scientific posters at AAIC 2025, and completing the transfer of all patent families to crystal buntanetap.

How many patients are currently enrolled in Annovis Bio's (ANVS) Alzheimer's trial?

38 patients are currently receiving buntanetap or placebo, with nearly 200 additional patients in the screening process.
Annovis Bio Inc

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49.69M
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Biotechnology
Pharmaceutical Preparations
United States
MALVERN