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Onkure Therapeutics OKUR · USD

Health Care · US listing · 🇺🇸 United States

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3.19

+11.15%

Close of 9 Nov 2026, in USD

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About Onkure Therapeutics

From its filings with the US Securities and Exchange Commission

SEC filings

Onkure Therapeutics is based in Boulder, Colorado and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker OKUR. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2024, it reported revenue of $0.

In its own words

OnKure Therapeutics, Inc. (“OnKure”, “we”, “us” or the “Company”) is a clinical-stage biopharmaceutical company focused on the discovery and development of precision medicines that target biologically validated drivers of cancers and other diseases that are underserved by available therapies. Using a structure-based drug design platform, we are committed to improving clinical outcomes for patients by building a pipeline of small molecule drugs designed to achieve optimal efficacy and tolerability by selectively targeting specific mutations shown to be key drivers of cancer and other diseases. By selectively sparing the wild-type enzyme and preferentially targeting the mutated form of the protein, which is oncogenic and drives disease processes in both cancer and vascular overgrowth syndromes, we aim to discover and develop drugs with improved safety and efficacy by sparing toxicity that arises from non-selective inhibition of the non-mutated (or wild-type) version of the protein. We work under the principle that inhibiting target proteins with specific mutations instead of wild-type variants should enable precise patient selection that will, in turn, improve the probability of clinical success. We designed our current product candidates utilizing disciplined medicinal chemistry, x-ray crystallography and computational chemistry to inhibit specified mutated versions of phosphoinositide 3-kinase alpha (“PI3Kα”), a key disease creating gene.

Quoted from its 10-K, filed 12 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
9 Apr 2021
Employees
55
Head office
6707 WINCHESTER CIRCLE, SUITE 400, BOULDER, CO, 80301
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
<br>Emerging growth company

Leadership

Pay as last reported

  • Dr. Andrew PhilipsIndependent Chairman of the Board$268,893
  • Dr. Nicholas SaccomanoPresident, Chief Executive Officer, Director, since 2024$9.5m
  • Mr. Jason LeveroneChief Financial Officer$2.7m
  • Dr. Dylan HartleyChief Scientific Officer
  • Mr. Michael GreyExecutive Director, since 2014$333,406
  • Dr. Samuel AgrestaChief Medical Officer$2.8m
  • Mr. R. Michael CarruthersIndependent Director$291,297
  • Ms. Valerie JansenIndependent Director$258,286
  • Dr. Isaac MankeIndependent Director$262,309
  • Mr. Edward MathersIndependent Director$296,578

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
36
Environment
37
Social
54
Governance
19
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

  • Onkure Therapeutics Inc focuses on rare genetic mitochondrial diseases with 55 employees.
  • Mavodelpar is a potent PPARd agonist targeting mitochondrial function and fatty acid oxidation.
  • Reneo Pharmaceuticals develops REN001 for primary mitochondrial myopathies and LC-FAOD diseases.

Weaknesses

  • The company has only 55 employees and limited resources for clinical development.
  • Reneo Pharmaceuticals is a clinical-stage company with no approved therapies yet.
  • Mavodelpar and REN001 are still in development without commercialization.

Opportunities

  • The US market offers opportunities for rare disease therapies with unmet medical needs.
  • Reneo Pharmaceuticals can expand into Europe for rare genetic mitochondrial disease treatments.
  • The growing focus on mitochondrial health provides new research avenues.

Threats

  • Competition from other biotech firms in the rare disease space is increasing.
  • Regulatory hurdles may delay approval for REN001 and mavodelpar.
  • The high cost of clinical trials could strain the company's financial resources.

Sources and methodology

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