217
Participants
Start Date
October 31, 2012
Primary Completion Date
April 30, 2016
Study Completion Date
April 30, 2016
OMP-59R5
OMP-59R5 administered intravenously
Gemcitabine
administered intravenously
Placebo
administered IV
Nab-Paclitaxel
administered intravenously
Memorial Sloan-Kettering Cancer Center, New York
Duke University Medical Center, Durham
Greenville Health System, Clinical Research Unit, Institute for Translational Oncology Research, Greenville
Northside Hospital, Inc. - GCS/Almex, Atlanta
Orlando Health, Inc., Orlando
Sarah Cannon Research Institute, Nashville
Cleveland Clinic, Cleveland
Oncology Hematology Care, Inc., Cincinnati
University of Michigan Health System, Ann Arbor
University of Wiscons in Hospi tal and Clinics, Madison
Allina Health, Virginia Piper Cancer Institute, Minneapolis
Washington University School of Medicine, St Louis
Peggy and Charles Stephenson Cancer Center, Oklahoma City
South Texas Accelerated Research Thereapeutics, LLC (START), San Antonio
Rocky Mountain Cancer Centers, Denver
Western Regional Medical Center, Inc., Goodyear
Comprehensive Cancer Centers ofNevada, Las Vegas
Ronald Reagan UCLA Medical Center, Drug Information Center, Department of Pharmaceutical Services, Los Angeles
Torrance Health Association Dba Torrance Memorial Physician Network/Cancer Care Associates, Redondo Beach
Pacific Shores Medical Group, Long Beach
St Jude Heritage Healthcare Virginia K. Crosson Cancer Center, Fullerton
CBCC Global Research, Inc. at Comprehensive Blood and Cancer Center, Bakersfield
Bend Memorial Clinic, Bend
Virginia Mason Medical Center, Seattle
Froedtert Hospital & Medical College of Wisconsin, Milwaukee
Beth Israel Deaconess Medical Center, Boston
Lead Sponsor
OncoMed Pharmaceuticals, Inc.
INDUSTRY