Dose-escalation Study of Birinapant and Pembrolizumab in Solid Tumors

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

August 4, 2017

Primary Completion Date

February 17, 2020

Study Completion Date

February 17, 2020

Conditions
Solid Tumors
Interventions
DRUG

Birinapant

Birinapant intravenous (IV) on Days 1 and 8 of each 21-Day Cycle. The following escalating doses of birinapant to be studied: 5.6, 11, 17, and 22 mg/m2. In the expansion phase the assigned recommended phase two dose will be administered in all cohorts

DRUG

Pembrolizumab

200 mg pembrolizumab IV on Day 1 of each 21-Day Cycle

Trial Locations (9)

19107

Thomas Jefferson University Sidney Kimmel Cancer Center, Philadelphia

21287

The Sidney Kimmel Comprehensive Cancer Center at John Hopkins, Baltimore

32763

Mid Florida Hematology and Oncology Center, Orange City

75251

Mary Crowley Cancer Research, Dallas

77030

MD Anderson Cancer Center, The University of Texas, Houston

85234

Banner MD Anderson Cancer Center, Gilbert

90048

Cedars-Sinai Medical Center, Los Angeles

90404

UCLA Dept of Medicine-Hematology/Oncology, Santa Monica

02215

Beth Israel Deaconess Medical Center, Boston

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

Medivir

INDUSTRY

NCT02587962 - Dose-escalation Study of Birinapant and Pembrolizumab in Solid Tumors | Biotech Hunter | Biotech Hunter