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ANVSNYSE

Annovis Bio, Inc.

Biopharma developer (SEC filing verified)·Phase 3·Malvern, PA, United States·CEO: Dr. Maria L. Maccecchini Ph.D.
Neurology

ANVS evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

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BioSniper AIPage evidence connected

Prepared research question

What matters most for ANVS—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ANVS

Annovis Bio, Inc. is a late-stage clinical company developing buntanetap for neurodegenerative diseases such as Alzheimer's and Parkinson's, with a focus on addressing unmet needs in aging populations.

Key risk: Insufficient capital runway

5.1/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$73.3M

Cash Runway

2.6 mo

Lead Asset

ANVS405 (Preclinical)

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 4 clinical trials · 3 catalysts for Annovis Bio, Inc..

AI OverviewAI overview is shown in English only.

Annovis Bio, Inc. is a late-stage clinical company developing buntanetap for neurodegenerative diseases such as Alzheimer's and Parkinson's, with a focus on addressing unmet needs in aging populations.

  • Annovis Bio is a late-stage clinical company addressing neurodegeneration, such as Alzheimer's disease [sec_mda · as of 2026-08-14].
  • The company's lead product candidate is buntanetap, targeting two large U.S. markets if approved [sec_mda · as of 2026-05-15].
  • As of 2026-06-30, the company reported cash and equivalents of $18.7 million, zero revenue, and a net loss of $14.8 million [sec].
  • The accumulated deficit was $181.3 million as of March 31, 2026 [sec_mda · as of 2026-05-15].
  • The company has never been profitable and expects losses to increase as it ramps up clinical development and commercial launch readiness [sec_mda · as of 2026-08-14].

What works

  • Annovis Bio is a late-stage clinical company with a product candidate, buntanetap, targeting two large U.S. markets in Alzheimer's and Parkinson's disease [sec_mda · as of 2026-05-15].
  • The company has ongoing clinical trials, including a Phase 3 topline readout expected in 2028, indicating progress in its development pipeline [catalyst_timeline].
  • The company has raised capital through equity offerings, such as $6.8 million in gross proceeds from stock sales in 2025 [sec_mda · as of 2026-03-13].

What to weigh

  • Annovis Bio has never been profitable and has incurred net losses since inception, with an accumulated deficit of $181.3 million as of March 31, 2026 [sec_mda · as of 2026-05-15].
  • The company does not have sufficient capital to fund operations for the next 12 months and will need to raise additional capital to meet obligations [sec_mda · as of 2026-05-15].
  • Cash and equivalents of $18.7 million as of 2026-06-30 may only fund operations until the fourth quarter of 2026, based on prior guidance [sec_mda · as of 2026-05-15].
  • The company faces risks from unforeseen expenses, difficulties, and delays in clinical trials, which could adversely affect its business [sec_mda · as of 2026-08-14].

From the filings

Quoted directly from source documents.

  • The company is a late-stage clinical company addressing neurodegeneration.

    We are a late-stage clinical company addressing neurodegeneration, such as Alzheimer's

    SEC MD&A · August 14, 2026

  • The company has never been profitable and has a significant accumulated deficit.

    We have never been profitable and have incurred net losses since inception. Our accumulated deficit at March 31, 2026 was $181.3 million.

    SEC MD&A · May 15, 2026

  • The company expects losses to increase as it ramps up clinical development.

    also expect these losses to further increase, as we ramp up our clinical development programs and begin activities for commercial launch readiness.

    SEC MD&A · August 14, 2026

  • The company does not have sufficient capital for the next 12 months.

    We do not have sufficient capital on hand to fund our operations for the next 12 months and will need to raise additional capital to meet our obligations as they become due.

    SEC MD&A · May 15, 2026

Catalyst timeline

  • 2028-06-01 · Phase3_Topline — Phase 3 Topline: A 6-month & 18-month Prospective, Randomized, Placebo-controlled, Double-blind Dual Clinical Trial IThis topline readout will provide efficacy and safety data for buntanetap in a dual trial setting.
  • 2029-11-01 · Phase3_Topline — Phase 3 Topline: An Open-label Clinical Trial Investigating the Long-term Safety of Buntanetap in Treating ParticipanThis open-label trial will assess long-term safety of buntanetap in participants.
  • 2030-05-01 · Phase3_Topline — Phase 3 Topline: An Open-label Clinical Trial Investigating the Long-term Safety of Buntanetap in Treating ParticipanThis additional open-label trial will further evaluate long-term safety of buntanetap.
Risks & what to watch (4)

Key risks

  • Insufficient capital runwayCash may only fund operations until Q4 2026; additional capital needed [sec_mda · as of 2026-05-15].
  • Clinical trial uncertaintiesUnforeseen expenses, delays, or difficulties in trials could harm business [sec_mda · as of 2026-08-14].
  • No approved products or revenueCompany has zero revenue and relies on future product approval [sec].
  • Regulatory and commercial risksAbility to obtain and maintain regulatory approval is uncertain [sec_mda · as of 2026-08-14].

What to watch

  • Phase 3 topline data for buntanetap expected in June 2028 [catalyst_timeline].
  • Ability to raise additional capital to extend cash runway beyond Q4 2026 [sec_mda · as of 2026-05-15].
  • Progress in patient enrollment and clinical trial execution for buntanetap [sec_mda · as of 2026-08-14].
  • Regulatory submissions and updates on approval pathways [sec_mda · as of 2026-08-14].

Sources: SEC MD&A · Generated August 27, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway0.7

2.6 months

Financial Health0.5

OCF -$22M · Net income -$15M

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst Momentum6.0

3 upcoming, next in ~641d

Insider Signal10.0

4 buys · 0 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

57

Total value held

$13.2M

Showing top 10 of 57 institutional holders of Annovis Bio, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
15.6%
Days to cover
3.7
Shares short
4,816,770
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ANVS short interest

Governance

Frequently asked questions

What is the AI investment thesis for Annovis Bio, Inc.?

Annovis Bio, Inc. is a late-stage clinical company developing buntanetap for neurodegenerative diseases such as Alzheimer's and Parkinson's, with a focus on addressing unmet needs in aging populations.

What is Annovis Bio, Inc.'s lead drug candidate?

Annovis Bio, Inc.'s most advanced tracked candidate is ANVS405 (Preclinical) for Traumatic brain injury and stroke.

What is Annovis Bio, Inc.'s next catalyst?

Annovis Bio, Inc.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A 6-month & 18-month Prospective, Randomized, Placebo-controlled, Double-blind Dual Clinical Trial I" — expected June 1, 2028.

Who is the CEO of Annovis Bio, Inc.?

Dr. Maria L. Maccecchini Ph.D. is the chief executive officer of Annovis Bio, Inc. (ANVS).

Where is Annovis Bio, Inc. headquartered?

Annovis Bio, Inc. (ANVS) is headquartered in Malvern, PA, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.