Tempest Therapeutics, Inc. — Cyborg Score 6/10

Solid
Oncology/Immuno-Oncology - Clinical Stage Biotechnology

Strategic Profile

Tempest differentiates through dual-mechanism small molecules designed to activate both tumor killing and immune responses, partnering with pharmaceutical leaders like Roche to de-risk development. The company recently acquired dual-targeting CAR-T programs from Factor Bioscience to expand its pipeline and extend runway while maintaining a capital-efficient strategy with partner-funded programs.

Cyborg Score Rationale

Tempest demonstrates solid fundamentals with a lead program showing clinical activity, strategic partnerships with Roche, recent pipeline expansion through CAR-T acquisition, and analyst support (average rating: Buy with $10.0 price target implying 311% upside). However, clinical-stage risk, cash burn concerns, and pre-revenue status moderate the score.

Top Insights

  • Lead program Amezalpat advancing in pivotal study with Roche, standard of care regimen in hepatocellular carcinoma with Phase 1b/2 data showing clinical activity
  • Recently acquired dual-targeting CAR-T programs (Feb 2026) designed to expand portfolio and extend cash runway with partner-funded development approach
  • Dual mechanism strategy: TPST-1120 (PPAR antagonist) and TPST-1495 (EP2/EP4 antagonist) both advancing Phase 1 trials as monotherapies and in combinations with approved agents
  • Achieved regulatory approvals including Fast Track and Orphan Drug designations for Amezalpat; China NMPA approval for pivotal trial (June 2025)

Named Competitors

  • Immuno-oncology small molecules — Traditional checkpoint inhibitors and targeted oncology therapies
  • CAR-T and cellular immunotherapy — Cell-based cancer therapies competing with Tempest's acquired CAR-T programs

Recent Developments

  • (February 2026) Announced strategic plan for recently acquired dual-targeting CAR-T assets from Factor Bioscience
  • (February 2026) Closed acquisition of dual-targeting CAR-T programs
  • (June 2025) Received China NMPA approval to proceed with pivotal trial for Amezalpat in combination with standard of care

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