172
Participants
Start Date
January 7, 2012
Primary Completion Date
April 18, 2017
Study Completion Date
May 8, 2017
OMP-59R5
OMP-59R5 administered intravenously
Etoposide
administered intravenously
Placebo
administered IV
Cisplatin or Carboplatin
administered intravenously
Memorial Sloan-Kettering Cancer Center, New York
Roswell Park Cancer Institute, Buffalo
UPMC Cancer Pavilion, Pittsburgh
Georgetown University Hospital, Washington D.C.
University of Maryland, Greenebaum Cancer Center, Baltimore
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore
Weinberg Cancer Institute, Baltimore
Virginia Cancer Specialists, Fairfax
Oncology and Hematology Associates of Southwest Virginia Inc., Blacksburg
Greenville Health System, Clinical Research Unit, Institute for Translational Oncology Research, Greenville
Piedmont Cancer Institute, Atlanta
Georgia Cancer Specialists, PC, Atlanta
Sarah Cannon, Fort Myers
Ocala Oncology Center, PL, Ocala
The Sarah Cannon Research Institute, Nashville
Tennessee Oncology, PLLC, Chattanooga
Norton Cancer Institute, Louisville
Case Western Reserve University, Cleveland
Oncology Hematology Care, Inc., Cincinnati
University of Michigan Medical Center, Clinical Trials Office, Ann Arbor
Karmanos Cancer Institute, Detroit
Minnesota Oncology Hematology , P.A., Minneapolis
Univeristy of Chicago Medical Center, Chicago
Oncology Hematology West PC, dba Nebraska Cancer Specialists, Omaha
Highlands Oncology Group, Rogers
Texas Oncology, P.A., Dallas
Texas Oncology-Bedford, Bedford
The University of Texas MD A nderson Cancer Center, Houston
Cancer Care Network of South Texas, San Antonio
Texas Oncology-South Austin, Austin
Rocky Mountain Cancer Centers, Denver
Cedars-Sinai Medical Center, Los Angeles
Providence Cancer Center Oncology and Hematology Care Eastside, Portland
Swedish Cancer Institute, Seattle
Yale University, New Haven
Lead Sponsor
OncoMed Pharmaceuticals, Inc.
INDUSTRY