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Clinical Trials/NCT00055562
NCT00055562
Completed
Phase 2

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

Celgene Corporation31 sites in 2 countries274 target enrollmentJanuary 2003

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Melanoma
Sponsor
Celgene Corporation
Enrollment
274
Locations
31
Status
Completed
Last Updated
20 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2003
End Date
December 2004
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (31)

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