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BIOAGE Labs BIOA · USD

Health Care · US listing · 🇺🇸 United States

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5.69

+6.55%

Close of 9 Nov 2026, in USD

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About BIOAGE Labs

From its filings with the US Securities and Exchange Commission

SEC filings

BIOAGE Labs is based in Emeryville, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker BIOA. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $9.0m and a net loss of $80.6m. At that date it held total assets of $294.9m and shareholders' equity of $272.1m.

In its own words

We are a clinical-stage biopharmaceutical company developing therapeutic product candidates for metabolic diseases by targeting the biology of human aging. Our technology platform and differentiated human datasets enable us to identify promising targets based on insights into molecular changes that drive aging.

In January 2025, we announced the nomination of our lead program, BGE-102, a potent, structurally novel, orally available, brain-penetrant small-molecule NLRP3 inhibitor. BGE-102 has a distinct mechanism and binding site from other NLRP3 inhibitors in development with issued patents covering both composition of matter and claims for the unique binding site.

In December 2025, we announced that BGE-102 was well-tolerated in Single Ascending Dose (SAD) and initial Multiple Ascending Dose (MAD) cohorts, with a pharmacokinetic profile supporting once-daily oral dosing, strong target engagement and high brain penetration.

We intend to advance BGE-102 in two therapeutic areas: cardiometabolic disease and ophthalmology.

Our first therapeutic area for BGE-102 is cardiometabolic disease, with a focus on atherosclerotic cardiovascular disease (ASCVD) risk reduction. Chronic systemic inflammation, as measured by high-sensitivity C-reactive protein (hsCRP), is an independent risk factor for cardiovascular events that is not adequately addressed by current lipid-lowering and antihypertensive therapies. In January 2026, we announced additional positive interim Phase 1 data, demonstrating potential for best-in-class hsCRP reduction in participants with elevated cardiovascular risk.

Quoted from its 10-K, filed 24 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Pharmaceuticals
Listed since
26 Sept 2024
Employees
60
Head office
5885 HOLLIS STREET, EMERYVILLE, CA, 94608
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
<br>Emerging growth company

Leadership

Pay as last reported

  • Dr. Jean-Pierre GarnierIndependent Chairman of the Board$1.5m
  • Dr. Kristen FortneyPresident, Chief Executive Officer, Director, since 2015$12.2m
  • Dr. Dov GoldsteinChief Financial Officer
  • Dr. Eric MorgenChief Operating Officer, Director, since 2017$2.5m
  • Dr. Paul RubinChief Medical Officer$1.9m
  • Dr. Michael DavidsonIndependent Director$492,400
  • Mr. Patrick EnrightIndependent Director$231,098
  • Dr. James HealyIndependent Director$233,339
  • Ms. Rekha HemrajaniIndependent Director$464,969
  • Dr. Vijay PandeIndependent Director

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
16
Environment
17
Social
16
Governance
14
Carbon reduction policy
No
Human rights policy
No

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Company operates in the Pharmaceuticals sector with a focus on metabolic diseases.
  • Lead product candidate azelaprag has shown positive results in Phase Ib trials.
  • Company has initiated Phase II trials for azelaprag in combination with tirzepatide.

Weaknesses

  • Company has only 60 employees, indicating limited resources.
  • IPO is scheduled for 2024-09-26, suggesting early-stage financial structure.
  • Company is clinical-stage, meaning products are not yet commercially available.

Opportunities

  • Potential for azelaprag to be used as an oral regimen with incretin drugs for obesity therapy.
  • Development of NLRP3 inhibitors for neuroinflammation diseases presents new market potential.
  • Preclinical programs based on human longevity data could lead to innovative treatments.

Threats

  • Clinical-stage status increases risk of trial failures or delays.
  • Competition in the pharmaceutical industry for obesity and metabolic disease treatments.
  • Dependence on successful clinical trials for product approval and market entry.

Sources and methodology

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Our data supplier
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