Overview
Phase 1/2 Study of Mocetinostat and Durvalumab in Patients With Advanced Solid Tumors and NSCLC
Status:
Terminated
Terminated
Trial end date:
2019-12-20
2019-12-20
Target enrollment:
0
0
Participant gender:
All
All
Summary
Mocetinostat (MGCD0103) is an orally administered HDAC inhibitor. Durvalumab (MEDI4736) is a human monoclonal antibody that is an inhibitor of the Programmed Cell Death Ligand (or PD-L1). Durvalumab is also known as a checkpoint inhibitor. This study is evaluating the combination regimen of mocetinostat and durvalumab in participants with Advanced or Metastatic Solid Tumors and Non-Small Cell Lung Cancer.Phase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Mirati Therapeutics Inc.Treatments:
Antibodies, Monoclonal
Durvalumab
Histone Deacetylase Inhibitors
Mocetinostat
Criteria
Inclusion Criteria:- Phase 1-Diagnosis of advanced or metastatic solid tumor; Phase 2-Diagnosis of NSCLC
- Not amenable to treatment with curative intent
- Adequate bone marrow and organ function
Exclusion Criteria:
- Impaired heart function
- Uncontrolled tumor in the brain
- Other active cancer