TPST-1120

Drug

Drug Profile

TPST-1120 is an investigational oral small-molecule selective PPAR-alpha antagonist being developed for advanced solid tumors, including hepatocellular carcinoma combinations with atezolizumab and bevacizumab. Company filings describe dual anti-tumor and immune-modulating effects and ongoing early-phase clinical development. It has no marketing approval.

Drug Class
Investigational oral selective PPAR-alpha antagonist
Approval Status
Investigational (ongoing Phase 1/2 development; no approved indication)
Mechanism of Action
Designed to block pathways supporting tumor proliferation, angiogenesis, and immune suppression, with both direct anti-proliferative and immune-modulating effects.
Indications
  • \Advanced or metastatic hepatocellular carcinoma in combination regimen studies (investigational)\
  • \Advanced solid tumors (investigational)\

Related News

Tempest Therapeutics Reports 2025 Financial Results and Clinical Progress

Tempest Therapeutics reported 2025 financial results showing $7.7 million in cash and highlighted clinical progress including 100% complete response rate in TPST-2003 CAR-T trial and multiple FDA designations for amezalpat in hepatocellular carcinoma. The company completed strategic CAR-T asset acquisition and plans Phase 2b registrational study for its lead program in 2026.

Related Clinical Trials

NCT ID Title Status Phase
NCT06680258

A Study of TPST-1120 With Atezolizumab Plus Bevacizumab in Patients With Unresectable or Metastatic HCC Not Previously Treated With Systemic Therapy

NOT_YET_RECRUITING PHASE3
NCT04524871

A Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Advanced Liver Cancers (Morpheus-Liver)

RECRUITING PHASE1/PHASE2