Founded Year

2015

Stage

IPO | IPO

Total Raised

$297M

Date of IPO

9/26/2024

Market Cap

0.28B

Stock Price

8.01

Revenue

$0000 

About BioAge

BioAge offers clinical-stage biotechnology focused on developing therapies for metabolic diseases by targeting human aging. It has programs aimed at treating conditions like obesity and related metabolic disorders. It serves the healthcare and pharmaceutical sectors with its drug discovery and development. It was founded in 2015 and is based in Richmond, California.

Headquarters Location

1445A South 50th Street

Richmond, California, 94804,

United States

510-806-1445

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BioAge's Products & Differentiators

    BGE-117

    (Please note that this and all drugs developed by BioAge are pre-market and have not yet been approved by FDA). BGE-117 is a HIF-PH inhibitor that activates hypoxia signaling, increasing the body’s ability to synthesize hemoglobin, the molecule that carries oxygen in the blood. Because BGE-117 targets a critical pathway that is dysregulated as we age, it holds great promise for anemia of aging as well as several acute and chronic conditions driven by muscle aging.

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Research containing BioAge

Get data-driven expert analysis from the CB Insights Intelligence Unit.

CB Insights Intelligence Analysts have mentioned BioAge in 4 CB Insights research briefs, most recently on Oct 22, 2025.

Expert Collections containing BioAge

Expert Collections are analyst-curated lists that highlight the companies you need to know in the most important technology spaces.

BioAge is included in 2 Expert Collections, including Digital Health.

D

Digital Health

12,122 items

The digital health collection includes vendors developing software, platforms, sensor & robotic hardware, health data infrastructure, and tech-enabled services in healthcare. The list excludes pureplay pharma/biopharma, sequencing instruments, gene editing, and assistive tech.

A

Artificial Intelligence (AI)

20,894 items

BioAge Patents

BioAge has filed 23 patents.

The 3 most popular patent topics include:

  • rare diseases
  • immune system
  • immunology
patents chart

Application Date

Grant Date

Title

Related Topics

Status

7/17/2023

2/4/2025

Inflammations, Rare diseases, Immune system, Immunology, Clusters of differentiation

Grant

Application Date

7/17/2023

Grant Date

2/4/2025

Title

Related Topics

Inflammations, Rare diseases, Immune system, Immunology, Clusters of differentiation

Status

Grant

Latest BioAge News

Northern District Of California Grants Motion To Dismiss Putative Class Action Against Biopharmaceutical Company

Nov 11, 2025

To embed, copy and paste the code into your website or blog: <iframe frameborder="1" height="620" scrolling="auto" src="//www.jdsupra.com/post/contentViewerEmbed.aspx?fid=35460487-7493-4f3a-a8f1-5e69d2c01259" style="border: 2px solid #ccc; overflow-x:hidden !important; overflow:hidden;" width="100%"></iframe> On October 30, 2025, Chief Judge Richard Seeborg of the United States District Court of the Northern District of California granted a motion to dismiss a putative securities class action alleging a biopharmaceutical company (the “Company”) and its officers (“Individual Defendants” and, collectively, “Defendants”) violated Sections 11 and 15 of the Securities Act of 1933 (the “Securities Act”). Soto v. BioAge Labs, Inc., et al., No. 25-cv-00196-RS (N.D. Cal. Oct. 30, 2025). Plaintiffs alleged that Defendants misled investors by omitting from risk disclosures an allegedly “inevitable” side-effect of the Company’s leading drug candidate. The Court dismissed the claims, finding (1) Defendants did not have any obligation under Section 11 to make the allegedly absent disclosure and (2) plaintiffs failed to plausibly allege the side-effect was inevitable. The Company holds an exclusive license to research, develop, and commercialize a weight-loss drug that is its leading product. Roughly two months before the Company’s initial public offering (“IPO”), it began a Phase 2 clinical trial on that drug. At the time of the IPO, the Company warned in its offering documents that “unexpected” or “atypical adverse events or side-effects” discovered during the ongoing trial could pose a risk to the Company and the drug’s developmental efforts. Approximately nine weeks after the IPO, the Company announced that some Phase 2 trial patients allegedly developed transaminitis (or elevated liver enzyme levels), prompting the Company to discontinue the trial and abandon the drug’s development. Plaintiffs alleged that transaminitis was a “typical” and “virtually certain” side-effect given the trial’s design and the drug’s properties and that Defendants’ failure to disclose this information caused their investments in the Company to suffer. The Court first held that, because the Company did not speak in its offering documents about transaminitis—or otherwise minimize a specific, known risk of the condition—Plaintiffs could not identify any statement rendered misleading by that alleged omission as required to state a Section 11 claim. The Court also rejected plaintiffs’ implication theory—that by disclosing possible “atypical” side-effects, the Company suggested no “typical” side effects posed a risk—as incompatible with In re Rigel Pharms., Inc., 687 F.3d 869 (9th Cir. 2012), which forecloses the notion an issuer must “disclose everything on a certain topic once [the issuer] disclose[s] anything on that topic” to avoid Section 11 liability. Separately, the Court held plaintiffs did not plead facts supporting a reasonable inference that transaminitis was “inevitable.” The Court found that the data from a pre-clinical animal study and the Phase 1 trial did not show transaminitis was likely, let alone “inevitable.” As to plaintiffs’ Phase 2 design-flaw allegations—such as that the Company enrolled participants who might have had elevated liver enzymes due to environmental and life-style factors—the Court found it could infer at most a possibility, not a near certainty, transaminitis would emerge to derail the trial. Concluding that the Section 11 claim failed, the Court did not address the Section 15 claim, but granted Plaintiffs leave to amend their complaint. Links & Downloads

BioAge Frequently Asked Questions (FAQ)

  • When was BioAge founded?

    BioAge was founded in 2015.

  • Where is BioAge's headquarters?

    BioAge's headquarters is located at 1445A South 50th Street, Richmond.

  • What is BioAge's latest funding round?

    BioAge's latest funding round is IPO.

  • How much did BioAge raise?

    BioAge raised a total of $297M.

  • Who are the investors of BioAge?

    Investors of BioAge include Felicis, Andreessen Horowitz, Amgen Ventures, RA Capital Management, Lilly Ventures and 23 more.

  • Who are BioAge's competitors?

    Competitors of BioAge include Brightseed and 4 more.

  • What products does BioAge offer?

    BioAge's products include BGE-117 and 2 more.

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