Melanoma Clinical Trial

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

Summary

Subjects are randomized to one of two treatment arms. All subjects are screened for eligibility within 28 days prior to randomization. The study consists of a treatment phase and a follow-up phase. Subjects will be treated in repeating 4 week cycles.

View Eligibility Criteria

Eligibility Criteria

Understand and voluntarily sign an informed consent form.
Able to adhere to the study visit schedule and other protocol requirements.
Metastatic malignant melanoma now stage IV, relapsed or refractory to standard metastatic therapy.
Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days of starting study drug.
Patients with active brain disease, or newly diagnosed brain metastases, within 4 weeks prior to the start of study treatment are excluded.

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

274

Study ID:

NCT00055562

Recruitment Status:

Completed

Sponsor:

Celgene Corporation

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There are 31 Locations for this study

See Locations Near You

University of Arizona Cancer Center
Tucson Arizona, 85724, United States
University of Southern California Norris Cancer Center
Los Angeles California, 90089, United States
UCLA
Los Angeles California, 90095, United States
St. Francis Memorial Hospital
San Francisco California, 94109, United States
Outpatient Clinic
Santa Monica California, 90404, United States
University of Colorado
Aurora Colorado, 80010, United States
The Harold Lever Regional Cancer Center
Waterbury Connecticut, 06708, United States
Lakeland Regional Cancer Center
Lakeland Florida, 33804, United States
Mount Sinai Comprehensive Cancer Center
Miami Beach Florida, 33140, United States
Lutheran General
Park Ridge Illinois, 60068, United States
Carle Clinic
Urbana Illinois, 61801, United States
Massachusetts General Hospital
Boston Massachusetts, 02214, United States
Beth Israel Deaconess Medical Ctr
Boston Massachusetts, 02215, United States
Spectrum Health
Grand Rapids Michigan, 49503, United States
Ellis Fischel Cancer Center
Columbia Missouri, 65203, United States
Washington University School of Medicine
St. Louis Missouri, 63110, United States
Melanoma Center of St Louis
St. Louis Missouri, 63131, United States
Biomedical Research Alliance of New York
New York New York, 10016, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10021, United States
The Linder Clinical Trial Center
Cincinnati Ohio, 45219, United States
Cleveland Clinic Foundation
Cleveland Ohio, 44195, United States
Penn State Hershey Medical Center
Hershey Pennsylvania, 17033, United States
UPMC Cancer Pavillion
Pittsburgh Pennsylvania, 15232, United States
Sarah Cannon Cancer Center
Nashville Tennessee, 37203, United States
MD Anderson Cancer Center
Houston Texas, 77030, United States
Tom Baker Cancer Center
Calgary Alberta, T2N 4, Canada
Cross Cancer Institute
Edmonton Alberta, T6G 1, Canada
Cancer Care Manitoba
Winnipeg Manitoba, R3E 0, Canada
Qell Health Sciences Center
Halifax Nova Scotia, B3H 2, Canada
Princess Margaret Hospital
Toronto Ontario, M5G 2, Canada
L'Hotel Dieu de Quebec
Quebec , PQ G1, Canada

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

274

Study ID:

NCT00055562

Recruitment Status:

Completed

Sponsor:


Celgene Corporation

How clear is this clinincal trial information?

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