222
Participants
Start Date
July 1, 2003
Primary Completion Date
October 1, 2006
Study Completion Date
March 1, 2007
CC-5013
CC-5013 - oral - 30mg daily on days 1-21 every 28 days
St. Vincent's Comprehensive Cancer Center, New York
SUNY Health Science Center at Brooklyn, Brooklyn
Western Pennsylvania Cancer Institute, Pittsburgh
Center for Cancer and Blood Disorders, Bethesda
Carolina Hematology-Oncology Associates, Charlotte
Northwest Georgia Oncology Centers, Marietta
Atlanta Cancer Care-Roswell, Roswell
Mayo Clinic, Jacksonville
Cleveland Clinic Myeloma Program Hematology & Medical Oncology /R35, Cleveland
Mayo Clinic, Rochester
Midwest Cancer Research Group, Skokie
Mayo Clinic, Scottsdale
Palo Verde Hematology Oncology, Glendale
Nevada Cancer Center, Las Vegas
Institute for Myeloma and Bone, Los Angeles
Cancer Care Associates, Redondo Beach
Providence St. Joseph Medical Center/Cancer Center, Burbank
Wilshire Oncology Medical Group, Inc., La Verne
Alta Bates Comprehensive Cancer Center, Berkeley
Swedish Cancer Institute, Seattle
Northwestern University Med Ctr, Chicago
University of Maryland Medical Center, Baltimore
Massachusetts General Hospital, Boston
Dana-Farber Cancer Institute, Boston
University of Massachusetts, Worcester
Fred Hutchinson Cancer Research Center, Seattle
Lead Sponsor
Celgene
INDUSTRY