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Spots Global Cancer Trial Database for Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects With Metastatic Malignant Melanoma

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Trial Identification

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

Official Title: Multicenter, Randomized, Controlled, Double-Blind, Parallel-Group Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects With Metastatic Malignant Melanoma Whose Disease Has Progressed on Treatment With DTIC, IL-2 or IFN Based Therapy

Study ID: NCT00055562

Interventions

CC 5013

Study Description

Brief 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.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Arizona Cancer Center, Tucson, Arizona, United States

University of Southern California Norris Cancer Center, Los Angeles, California, United States

UCLA, Los Angeles, California, United States

St. Francis Memorial Hospital, San Francisco, California, United States

Outpatient Clinic, Santa Monica, California, United States

University of Colorado, Aurora, Colorado, United States

The Harold Lever Regional Cancer Center, Waterbury, Connecticut, United States

Lakeland Regional Cancer Center, Lakeland, Florida, United States

Mount Sinai Comprehensive Cancer Center, Miami Beach, Florida, United States

Lutheran General, Park Ridge, Illinois, United States

Carle Clinic, Urbana, Illinois, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Ctr, Boston, Massachusetts, United States

Spectrum Health, Grand Rapids, Michigan, United States

Ellis Fischel Cancer Center, Columbia, Missouri, United States

Washington University School of Medicine, St. Louis, Missouri, United States

Melanoma Center of St Louis, St. Louis, Missouri, United States

Biomedical Research Alliance of New York, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

The Linder Clinical Trial Center, Cincinnati, Ohio, United States

Cleveland Clinic Foundation, Cleveland, Ohio, United States

Penn State Hershey Medical Center, Hershey, Pennsylvania, United States

UPMC Cancer Pavillion, Pittsburgh, Pennsylvania, United States

Sarah Cannon Cancer Center, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Tom Baker Cancer Center, Calgary, Alberta, Canada

Cross Cancer Institute, Edmonton, Alberta, Canada

Cancer Care Manitoba, Winnipeg, Manitoba, Canada

Qell Health Sciences Center, Halifax, Nova Scotia, Canada

Princess Margaret Hospital, Toronto, Ontario, Canada

L'Hotel Dieu de Quebec, Quebec, , Canada

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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