Phase 1/2 Study of Mocetinostat and Durvalumab in Patients With Advanced Solid Tumors and NSCLC
Stopped The study was discontinued early because the Sponsor de-prioritized development of mocetinostat. The decision to stop was not due to any patient safety issues.
Conditions
Interventions
- DRUG: Mocetinostat - 50 mg
- DRUG: Mocetinostat - 70 mg
- DRUG: Mocetinostat - 90 mg
- DRUG: Mocetinostat - Recommended Phase 2 Dose (70 mg)
- DRUG: Durvalumab - 1500 mg
Sponsor
Mirati Therapeutics Inc.