Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects With Metastatic Malignant Melanoma

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

274

Participants

Timeline

Start Date

January 31, 2003

Study Completion Date

December 31, 2004

Conditions
MelanomaNeoplasm Metastasis
Interventions
DRUG

CC 5013

Trial Locations (31)

10016

Biomedical Research Alliance of New York, New York

10021

Memorial Sloan Kettering Cancer Center, New York

15232

UPMC Cancer Pavillion, Pittsburgh

33140

Mount Sinai Comprehensive Cancer Center, Miami Beach

44195

Cleveland Clinic Foundation, Cleveland

45219

The Linder Clinical Trial Center, Cincinnati

49503

Spectrum Health, Grand Rapids

61801

Carle Clinic, Urbana

63110

Washington University School of Medicine, St Louis

63131

Melanoma Center of St Louis, St Louis

65203

Ellis Fischel Cancer Center, Columbia

80010

University of Colorado, Aurora

85724

University of Arizona Cancer Center, Tucson

90089

University of Southern California Norris Cancer Center, Los Angeles

90404

Outpatient Clinic, Santa Monica

94109

St. Francis Memorial Hospital, San Francisco

90095-6956

UCLA, Los Angeles

06708

The Harold Lever Regional Cancer Center, Waterbury

33804-1057

Lakeland Regional Cancer Center, Lakeland

60068-1270

Lutheran General, Park Ridge

02214-2698

Massachusetts General Hospital, Boston

02215-5400

Beth Israel Deaconess Medical Ctr, Boston

17033-0850

Penn State Hershey Medical Center, Hershey

37203-1632

Sarah Cannon Cancer Center, Nashville

77030-4009

MD Anderson Cancer Center, Houston

T2N 4N2

Tom Baker Cancer Center, Calgary

T6G 1Z2

Cross Cancer Institute, Edmonton

R3E 0V9

Cancer Care Manitoba, Winnipeg

B3H 2y9

Qell Health Sciences Center, Halifax

M5G 2M9

Princess Margaret Hospital, Toronto

PQ G1R 2J6

L'Hotel Dieu de Quebec, Québec

Sponsors
All Listed Sponsors
lead

Celgene Corporation

INDUSTRY