Overview

Phase 1/2 Study of Mocetinostat and Durvalumab in Patients With Advanced Solid Tumors and NSCLC

Status:
Terminated
Trial end date:
2019-12-20
Target enrollment:
0
Participant gender:
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 2
Accepts Healthy Volunteers?
No
Details
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