Tempest Therapeutics
Tempest Therapeutics is a clinical-stage, pre-revenue biotechnology company (NASDAQ: TPST) developing oral small molecule and CAR-T cell therapies for patients with advanced or relapsed/refractory cancers, advancing amezalpat, TPST-1495, TREX-1 and the acquired TPST-2003 CD19/BCMA CAR-T franchise via partner-driven development.
- Company typePublic
- Founded2011
- HeadquartersSan Francisco, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Tempest Therapeutics does
Tempest Therapeutics (NASDAQ: TPST) is a clinical-stage biotechnology company headquartered in Brisbane, California, developing oral small molecule therapeutics and CAR-T cell therapies for patients with advanced or relapsed/refractory cancers. The pipeline is anchored by amezalpat (TPST-1120), an oral PPARα antagonist being advanced toward pivotal Phase 3 development in first-line hepatocellular carcinoma, and includes TPST-1495 (a dual EP2/EP4 prostaglandin receptor antagonist in familial adenomatous polyposis, operationalized by the NCI Cancer Prevention Network), a TREX1 program, and — added in February 2026 through the all-stock acquisition of Factor Bioscience and Erigen — a CAR-T franchise led by TPST-2003 (dual-targeting CD19/BCMA), the in vivo CAR-T alternative TPST-4003, and allogeneic candidates TPST-2206, TPST-3003 and TPST-3206 being developed in China with Novatim Immune Therapeutics.
The business model is pre-revenue: Tempest has no commercial product and no product pricing, generates no product revenue, and funds operations through repeated equity financings (a $15M private placement in April 2022, ~$4.6M in June 2025, ~$4.25M upfront/up to $8.35M in November 2025, ~$2M in March 2026 and ~$2M via warrant exercise in May 2026, with H.C. Wainwright as recurring placement agent). Go-to-market is partner-driven: clinical development is operationalized by Novatim (China), the NCI Cancer Prevention Network (FAP), and Cincinnati Children's AGCTC (manufacturing), and patient access to investigational therapy is restricted to clinical trial enrollment under the company's Expanded Access Policy. The company is publicly traded, micro-cap (~$18.65M market cap, down ~82% YoY), and as of Q1 2026 carried $1.8M in cash against $27.7M in net loss, $822,000 in stockholders' equity, and an active Nasdaq deficiency notice for failing the $2.5M minimum equity requirement — a going-concern signal it disclosed in conjunction with its March 2026 private placement.
Customers are not commercial in the traditional sense. End users are oncology patients with limited treatment options — relapsed/refractory multiple myeloma, POEMS syndrome, first-line HCC, RCC, CCA, and FAP — accessed only through clinical trials. Strategic counterparties (Novatim, NCI, Cincinnati Children's, H.C. Wainwright, EcoR1 Capital, Versant Venture Capital) effectively constitute the B2B "customer" base, with a planned out-licensing/partnership for amezalpat Phase 3 explicitly tied to the product's commercial pathway.
Tempest Therapeutics firmographics
Firmographics- Name
- Tempest Therapeutics
- Legal name
- Tempest Therapeutics, Inc.
- Website
- https://tempesttx.com
- Company type
- Public
- Founded year
- 2011
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Tempest Therapeutics is a clinical-stage, pre-revenue biotechnology company (NASDAQ: TPST) developing oral small molecule and CAR-T cell therapies for patients with advanced or relapsed/refractory cancers, advancing amezalpat, TPST-1495, TREX-1 and the acquired TPST-2003 CD19/BCMA CAR-T franchise via partner-driven development.
- Ownership category
- akta.pro rank
Tempest Therapeutics industry classification
Industry- Product category
- Clinical-stage oncology therapeutics
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- CAR-T & TCR-T Therapies (HLAAABAC)
- akta.pro secondary industry
- Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches) (HLAAACAF)
Keywords
Where Tempest Therapeutics is headquartered
LocationHeadquarters
- HQ city
- San Francisco
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Tempest Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Supply Chain, Others
Revenue model
- Pre-revenue / No commercial product revenue: Clinical-stage biotechnology company with no commercial products; no product revenue generated. Operations are funded by equity financings (private placements, registered direct offerings, warrant exercises) and capital is used for R&D and general corporate purposes. The company reported a 2025 net loss of $26.3 million and Q1 2026 net loss of $27.7 million driven primarily by a $22.1 million acquired in-process R&D charge from the Factor Bioscience asset acquisition.
Go-to-market motion1 record
Distribution channels4 records
Marketing channels5 records
Tempest Therapeutics product offering
Product offeringCore offering
Tempest Therapeutics is a clinical-stage biotechnology company developing a portfolio of oral small molecule therapeutics and CAR-T cell therapies designed to treat cancer through direct tumor killing, immune activation, or a combination of both mechanisms. The lead asset is amezalpat (TPST-1120), an oral PPARα antagonist advancing toward pivotal development for first-line hepatocellular carcinoma, supplemented by TPST-1495 (dual EP2/EP4 antagonist) for familial adenomatous polyposis, TREX-1 (STING-pathway activator), and an acquired CAR-T franchise led by TPST-2003, a dual-targeting CD19/BCMA CAR-T for relapsed/refractory multiple myeloma and POEMS syndrome.
Product overview
Tempest Therapeutics is a clinical-stage biotechnology company developing a portfolio of oral small molecule therapeutics and CAR-T cell therapies designed to treat cancer through direct tumor killing, activation of tumor-specific immunity, or a combination of both mechanisms. The lead asset is amezalpat (TPST-1120), an oral PPARα antagonist advancing toward pivotal Phase 3 development for first-line hepatocellular carcinoma (HCC). The small molecule pipeline also includes TPST-1495, a dual EP2/EP4 prostaglandin receptor antagonist for familial adenomatous polyposis (FAP) under NCI's Cancer Prevention Network, and TREX-1, a STING-pathway TREX1 inhibitor. Following the February 2026 all-stock acquisition of Factor Bioscience and Erigen, Tempest added a CAR-T cell therapy franchise led by TPST-2003 (ERI-2003), a dual-targeting CD19/BCMA CAR-T for relapsed/refractory multiple myeloma, supported by next-generation candidates TPST-4003 (in vivo CAR-T) and TPST-2206, TPST-3003, and TPST-3206 (allogeneic CAR-Ts being developed in China with Novatim Immune Therapeutics). Together these programs comprise Tempest's oncology pipeline targeting advanced cancers in patients who have failed or relapsed from prior therapies.
Differentiator
Problem solved
Functional benefit
Brands
- amezalpat (TPST-1120): Lead small molecule therapeutic candidate for first-line hepatocellular carcinoma (HCC), being developed toward pivotal Phase 3 development.
- TPST-1495
- TPST-2003
Products and services
- Amezalpat (TPST-1120) Oral PPARα antagonist designed to treat cancer through direct tumor killing and tumor-specific immune activation. Lead clinical-stage asset for first-line hepatocellular carcinoma (HCC), with prior clinical evaluation in renal cell carcinoma (RCC) and cholangiocarcinoma (CCA).
- TPST-1495 Dual EP2/EP4 prostaglandin receptor antagonist in development for familial adenomatous polyposis (FAP), designed to modulate prostaglandin-driven immune suppression in the tumor microenvironment. Phase 2 to be operationalized by the NCI Cancer Prevention Network.
- TREX-1 TREX1 inhibitor targeting the STING (stimulator of interferon genes) innate immune pathway to activate tumor-specific immunity; included in Tempest's portfolio of oral cancer therapeutics.
- TPST-2003 (ERI-2003) Clinical-stage dual-targeting CD19/BCMA CAR-T cell therapy for relapsed/refractory multiple myeloma (rrMM) and POEMS syndrome, acquired from Factor Bioscience Inc. and Erigen LLC in February 2026. Demonstrated 100% complete response rate in 15 CAR-T-naïve efficacy-evaluable patients across REDEEM-1 and POEMS-1 Phase 1 trials, with no Grade >3 CRS or ICANS across 44 patients treated to date.
- TPST-4003 In vivo CAR-T alternative being developed as part of Tempest's post-acquisition dual CAR-T strategy, expanding beyond ex vivo cell therapy modalities.
- TPST-2206, TPST-3003, TPST-3206 Pipeline of next-generation allogeneic CAR-T cell therapy candidates; clinical development in China to be operationalized by Novatim Immune Therapeutics (Zhejiang) Co., Ltd.
Quantifiable outcome
- 100% complete response rate across 15 CAR-T-naïve efficacy evaluable patients in REDEEM-1 and POEMS-1 trials with TPST-2003
- +3 more outcomes
Companies that use Tempest Therapeutics
Customer profileSegments3 records
Ideal customer profiles3 records
Tempest Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature6 records
Tempest Therapeutics partnerships and signals
Strategic signalPartnerships
Five partnerships are on record, tiered core and flagship.
- Cincinnati Children's Applied Gene and Cell Therapy Center (AGCTC)coreSelected as Tempest's lead contract development and manufacturing partner to conduct technology transfer for TPST-2003, the company's dual-targeting CD19/BCMA CAR-T therapy for relapsed/refractory multiple myeloma. Partnership follows positive interim data from REDEEM-1 Phase 1/2a trial showing 100% complete response in all six efficacy evaluable patients. All IND-enabling activities are planned to be complete by Q3 2026 to support a potential IND filing in Q4 2026 for a planned U.S. registrational study.
- Factor Bioscience Inc.flagshipTempest closed its all-stock acquisition of dual-targeting CAR-T programs from Factor Bioscience (and affiliates, including Erigen LLC) on February 5, 2026, following stockholder approval on January 27, 2026. The transaction brought Tempest a clinical-stage CD19/BCMA CAR-T candidate (TPST-2003/ERI-2003) with a planned BLA filing in China for 2027, extended operational runway to mid-2027, and brought in Factor's co-founder Dr. Matt Angel as President and CEO of Tempest. Existing Tempest shareholders retained approximately 35% of the pro forma company.
- Erigen LLCcoreCo-seller (with Factor Bioscience) of dual-targeting CAR-T programs acquired by Tempest in an all-stock transaction completed in February 2026. Asset acquisition included TPST-2003 (CD19/BCMA CAR-T) along with other next-generation CAR-T programs. The transaction generated a $22.1 million acquired in-process R&D charge in Q1 2026.
- Novatim Immune Therapeutics (Zhejiang) Co., Ltd.flagshipOperationalizes China clinical development of TPST-2003, TPST-2206, TPST-3003, TPST-3206, and TPST-4003 CAR-T candidates. Strategic partner supporting the planned registrational Phase 2b in China for TPST-2003 by end of 2026 and the planned BLA filing in China in 2027.
- National Cancer Institute (NCI) Cancer Prevention NetworkcoreOperationalizes the TPST-1495 Phase 2 clinical development in familial adenomatous polyposis (FAP). Government-sponsored research network providing clinical infrastructure and operational expertise for the FAP program.
Scale indicators10 records
Recent moves6 records
Expansion highlights6 records
Tempest Therapeutics competitors and assessment
Company assessmentDirect peers
- Caribou Biosciences: Clinical-stage cell therapy company developing allogeneic CAR-T candidates (e.g., CB-010, CB-011) in oncology indications including hematologic malignancies. Directly comparable to Tempest in modality (allogeneic CAR-T), clinical-stage status, and pipeline focus on dual-targeting and next-generation cell therapy.
- Allogene Therapeutics: Clinical-stage cell therapy company pioneering allogeneic CAR-T (e.g., cemacabtagene ansegedleucel). Directly comparable to Tempest in modality (allogeneic CAR-T), oncology focus, and clinical-stage profile; both companies are pursuing next-generation cell therapy to overcome limitations of approved autologous CAR-Ts.
- CRISPR Therapeutics: Clinical-stage gene-editing company developing gene-edited allogeneic CAR-T therapies (e.g., CTX112) in oncology. Directly comparable to Tempest in clinical-stage cell therapy, oncology pipeline, and pursuit of next-generation engineered CAR-T modalities.
- Atara Biotherapeutics: Clinical-stage cell therapy company developing allogeneic T-cell and CAR-T therapies (e.g., tabelecleucel) for oncology and autoimmune indications. Comparable to Tempest in pre-commercial cell therapy focus, micro-cap status, and reliance on partnership-driven development.
- Cellectis: Clinical-stage gene-editing and cell therapy company developing allogeneic CAR-T candidates (e.g., UCART19) using its TALEN-based gene-editing platform. Directly comparable to Tempest in clinical-stage allogeneic CAR-T development and oncology focus.
- Precision BioSciences: Clinical-stage gene-editing and cell therapy company developing in vivo gene-editing and allogeneic CAR-T programs (e.g., PBCAR19B, PBCAR269A). Directly comparable to Tempest in next-generation cell therapy and in vivo modality exploration.
- Editas Medicine: Clinical-stage gene-editing and cell therapy company developing CRISPR-based ex vivo (CTX112 partnership) and in vivo (reni-cel) therapies. Comparable to Tempest in gene-editing/cell-therapy focus, clinical-stage status, and small-cap public-company profile.
- 2seventy bio: Cell therapy company developing Abecma (idecabtagene vicleucel) BCMA-directed CAR-T for multiple myeloma in partnership with Bristol Myers Squibb. Directly comparable to Tempest in BCMA CAR-T focus for multiple myeloma — a key competitive reference point for TPST-2003.
Broad incumbents
- Foghorn Therapeutics: Clinical-stage oncology company developing small molecule therapeutics targeting the chromatin regulatory system. Comparable to Tempest in small molecule oncology focus and clinical-stage public-company status, though Foghorn operates in a different mechanism space (chromatin biology vs. PPARα/EP2-EP4/TREX1).
- Bristol Myers Squibb: Large biopharmaceutical company with an established CAR-T franchise (Breyanzi, Abecma) and a broad oncology pipeline. Relevant to Tempest as a potential strategic acquirer/partner for TPST-2003 (BCMA CAR-T competing with Abecma) and as the broader commercial benchmark for next-generation CAR-T development.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks7 records
Key highlights6 records
Customer concentration
Tempest Therapeutics social profiles
Digital presenceTempest Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Tempest Therapeutics leadership team
Management profileNumber of profiles
Profiles10 records
Tempest Therapeutics subsidiaries and ownership
Company hierarchySubsidiaries1 record
Tempest Therapeutics funding detail
Funding detailFunding overview
Funding rounds9 records
Investors8 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Tempest Therapeutics M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Tempest Therapeutics
What does Tempest Therapeutics do?
Tempest Therapeutics is a clinical-stage biotechnology company developing a portfolio of oral small molecule therapeutics and CAR-T cell therapies designed to treat cancer through direct tumor killing, immune activation, or a combination of both mechanisms. The lead asset is amezalpat (TPST-1120), an oral PPARα antagonist advancing toward pivotal development for first-line hepatocellular carcinoma, supplemented by TPST-1495 (dual EP2/EP4 antagonist) for familial adenomatous polyposis, TREX-1 (STING-pathway activator), and an acquired CAR-T franchise led by TPST-2003, a dual-targeting CD19/BCMA CAR-T for relapsed/refractory multiple myeloma and POEMS syndrome.
Is Tempest Therapeutics a public or private company?
Tempest Therapeutics is a public company. It is classified as public and is currently operating.
When was Tempest Therapeutics founded?
Tempest Therapeutics was founded in 2011. It employs 11 to 50 people.
Where is Tempest Therapeutics based?
Tempest Therapeutics is headquartered in San Francisco, United States, in the North America region.
How does Tempest Therapeutics make money?
One revenue line is on record: pre-revenue / No commercial product revenue.
Who are Tempest Therapeutics's main competitors?
Direct peers on record are Caribou Biosciences, Allogene Therapeutics, CRISPR Therapeutics, Atara Biotherapeutics, Cellectis, Precision BioSciences, Editas Medicine and 2seventy bio. Broad incumbents are Foghorn Therapeutics and Bristol Myers Squibb.
Does Tempest Therapeutics have an API?
No public API is recorded for Tempest Therapeutics.
What industry is Tempest Therapeutics in?
Tempest Therapeutics's product category is Clinical-stage oncology therapeutics. Its primary akta.pro industry code is HLAAABAC, CAR-T & TCR-T Therapies, with a secondary code of HLAAACAF, Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches). Its SIC code is 2834.