Safety and Efficacy of Single-agent CC-5013 in Subjects With Relapsed and Refractory Multiple Myeloma

PHASE2CompletedINTERVENTIONAL
Enrollment

222

Participants

Timeline

Start Date

July 1, 2003

Primary Completion Date

October 1, 2006

Study Completion Date

March 1, 2007

Conditions
Multiple Myeloma
Interventions
DRUG

CC-5013

CC-5013 - oral - 30mg daily on days 1-21 every 28 days

Trial Locations (26)

10011

St. Vincent's Comprehensive Cancer Center, New York

11203

SUNY Health Science Center at Brooklyn, Brooklyn

15224

Western Pennsylvania Cancer Institute, Pittsburgh

20717

Center for Cancer and Blood Disorders, Bethesda

28203

Carolina Hematology-Oncology Associates, Charlotte

30060

Northwest Georgia Oncology Centers, Marietta

30076

Atlanta Cancer Care-Roswell, Roswell

32224

Mayo Clinic, Jacksonville

44195

Cleveland Clinic Myeloma Program Hematology & Medical Oncology /R35, Cleveland

55902

Mayo Clinic, Rochester

60077

Midwest Cancer Research Group, Skokie

85259

Mayo Clinic, Scottsdale

85304

Palo Verde Hematology Oncology, Glendale

89109

Nevada Cancer Center, Las Vegas

90067

Institute for Myeloma and Bone, Los Angeles

90277

Cancer Care Associates, Redondo Beach

91505

Providence St. Joseph Medical Center/Cancer Center, Burbank

91750

Wilshire Oncology Medical Group, Inc., La Verne

94704

Alta Bates Comprehensive Cancer Center, Berkeley

98104

Swedish Cancer Institute, Seattle

60611-2927

Northwestern University Med Ctr, Chicago

21201-1595

University of Maryland Medical Center, Baltimore

02114

Massachusetts General Hospital, Boston

02115

Dana-Farber Cancer Institute, Boston

01655

University of Massachusetts, Worcester

98109-1024

Fred Hutchinson Cancer Research Center, Seattle

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY