Melanoma Clinical Trial

Phase II, 2nd Line Melanoma – RAND Monotherapy

Summary

The main purpose of this study is to estimate the proportion of patients with a type of skin cancer called melanoma who are progression free, (that is, the cancer has not gotten substantially worse), when treated with Anti-CD137 (4-1BB) (BMS-663513) at 0.1 mg/kg, 1 mg/kg or 5 mg/kg every 3 weeks or 1 mg/kg every 6 weeks

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subjects must have been previously treated with one line of systemic anti-cancer therapy (non-experimental or experimental) for metastatic disease, and relapsed, failed to respond (CR or PR) or did not tolerate that regimen. If the treatment has been administered as an adjuvant and/or neoadjuvant therapy, the subject must have documented disease progression from the last treatment and also received one additional line of systemic therapy for metastatic disease.
Men and women, who are at least 18 years of age

Exclusion Criteria:

Ocular or mucosal melanoma
Complete surgical resection of all identifiable sites of disease
Symptomatic brain metastasis. Subjects with signs or symptoms suggestive of brain metastasis are not eligible unless brain metastases are ruled out by computerized axial tomography (CT) scan or magnetic resonance imaging (MRI). Subjects with stable brain metastasis and those who were previously treated with radiotherapy or surgery must have no current evidence of symptomatic brain metastasis and are off steroid therapy for at least 4 weeks prior to randomization

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

158

Study ID:

NCT00612664

Recruitment Status:

Completed

Sponsor:

Bristol-Myers Squibb

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There are 32 Locations for this study

See Locations Near You

The Angeles Clinic & Research Institute
Los Angeles California, 90025, United States
Yale University School Of Medicine
New Haven Connecticut, 06520, United States
Oncology Specialists, S.C.
Park Ridge Illinois, 60068, United States
Indiana University Melvin And Bren Simon Cancer Center
Indianapolis Indiana, 46202, United States
Harry & Jeanette Weinberg Cancer Inst At Franklin Square
Baltimore Maryland, 21237, United States
Dana-Farber Cancer Inst
Boston Massachusetts, 02115, United States
Mem Sloan-Ket Can Ctr
New York New York, 10021, United States
Blumenthal Cancer Center, Carolinas Medical Center
Charlotte North Carolina, 28204, United States
Providence Portland Medical Center
Portland Oregon, 97213, United States
University Of Texas
Houston Texas, 77030, United States
Local Institution
Calgary Alberta, T2N 4, Canada
Local Institution
Edmonton Alberta, T6G 1, Canada
Local Institution
Montreal Quebec, H4J 1, Canada
Local Institution
Aarhus C , 8000, Denmark
Local Institution
Odense C , DK-50, Denmark
Local Institution
Lille , 59037, France
Local Institution
Paris Cedex 13 , 75651, France
Local Institution
Paris , 75010, France
Local Institution
Vandoeuvre Les Nancy , 54511, France
Local Institution
Villejuif , 94805, France
Local Institution
Homburg / Saar , 66421, Germany
Local Institution
Jena , 07740, Germany
Local Institution
Kiel , 24105, Germany
Local Institution
Mainz , 55131, Germany
Local Institution
Mannheim , 68167, Germany
Local Institution
Tubingen , 72076, Germany
Local Institution
Wuerzburg , 97080, Germany
Local Institution
Genove , 16132, Italy
Local Institution
Milano , 20141, Italy
Local Institution
Napoli , 80131, Italy
Local Institution
Padova , 35128, Italy
Local Institution
Siena , 53100, Italy

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

158

Study ID:

NCT00612664

Recruitment Status:

Completed

Sponsor:


Bristol-Myers Squibb

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