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Tempest Therapeutics TPST · USD

Health Care · US listing · 🇺🇸 United States

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0.36

-5.04%

Close of 9 Nov 2026, in USD

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About Tempest Therapeutics

From its filings with the US Securities and Exchange Commission

SEC filings

Tempest Therapeutics is based in Brisbane, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker TPST. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2017, it reported revenue of $295,000.

In its own words

We are a clinical-stage biotechnology company advancing a diversified portfolio of cell therapy and small molecule product candidates. In February 2026, we expanded our pipeline through a strategic transaction under which we acquired rights to a portfolio of dual-targeting chimeric antigen receptor T-cells (“CAR-T”) product candidates with the potential to treat certain blood cancers, solid tumors and immunology indications, including TPST-2003, an autologous CD19/B-cell maturation antigen (“BCMA”) CAR-T therapy currently in clinical development for relapsed or refractory multiple myeloma (“rrMM”).

Our portfolio also includes two clinical-stage small molecule product candidates with the potential to treat certain cancer indications. One of our small-molecule product candidates, amezalpat (previously known as TPST-1120), has completed a Phase 2 study in first-line hepatocellular carcinoma (“HCC”). Amezalpat remains Phase 3-ready in HCC and we plan to pursue business development discussions to advance pivotal development. Our second small-molecule product candidate is TPST-1495, which we plan to initiate a Phase 2 study for in familial adenomatous polyposis (“FAP”), with first patient enrollment expected in 2026. The study is expected to be funded by the National Cancer Institute (“NCI”) and conducted through the Cancer Prevention Clinical Trials Network (“CP-CTNet”), enabling advancement with limited internal capital deployment.

Quoted from its 10-K, filed 30 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
4 Oct 2012
Employees
19
Head office
2000 SIERRA POINT PARKWAY, BRISBANE, CA, 94005
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Mr. Stephen BradyChairman of the Board, since 2021$1.9m
  • Dr. Matthew AngelPresident, Chief Executive Officer, Director, since 2026
  • Mr. Nicholas MaestasChief Financial Officer, Head - Corporate Strategy, Corporate Secretary$622,095
  • Dr. Samuel WhitingExecutive Vice President, Chief Medical Officer$1.1m
  • Ms. Christine PellizzariIndependent Director$95,403
  • Mr. Michael RaabIndependent Director$145,903
  • Dr. Ronit SimantovIndependent Director$88,403

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
21
Environment
24
Social
14
Governance
26
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

  • Clinical-stage biotechnology company with two active drug programs in Phase I/II trials.
  • TPST-1120 targets PPARa for solid tumors with global Phase Ib/II trials in HCC.
  • TPST-1495 is a dual EP2/EP4 antagonist in Phase I trials for solid tumors.

Weaknesses

  • 19 full-time employees indicate limited workforce capacity for development.
  • Headquartered in Brisbane California, a small city with limited biotech infrastructure.
  • IPO in 2012 suggests long development timeline without significant revenue.

Opportunities

  • Expanding clinical trials for TPST-1120 in combination with atezolizumab and bevacizumab globally.
  • Growing demand for targeted cancer therapies in the Health Care sector.
  • Potential partnerships with larger biotech firms for drug development.

Threats

  • Competition from established biotech companies in the Health Care sector.
  • Regulatory delays in clinical trials for cancer drugs.
  • Dependence on successful Phase I/II trial results for future funding.

Sources and methodology

Data on this tab
Our data supplier
Chart on the Overview
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