CompletedPhase 2NCT00106431
A Single Agent Phase II Study of Romidepsin (Depsipeptide, FK228) in the Treatment of Cutaneous T-cell Lymphoma (CTCL)
Studying Aggressive primary cutaneous T-cell lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celgene
- Principal Investigator
- Jean Nichols, Ph.D.Gloucester Pharmaceuticals, Inc.
- Intervention
- romidepsin (depsipeptide, FK228)(drug)
- Enrollment
- 102 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2005 – 2008
Study locations (11)
- UCLA Jonsson Cancer Center, Los Angeles, California, United States
- Stanford Comprehensive Cancer Center, Stanford, California, United States
- Boston Medical Center, Boston, Massachusetts, United States
- University of Pennsylvania Abrahamson Cancer Center, Philadelphia, Pennsylvania, United States
- Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States
- MD Anderson Cancer Center, Houston, Texas, United States
- Research Site, Multiple Locations, France
- Research Site, Multiple Locations, Germany
- Research Site, Multiple Locations, Poland
- Research Site, Multiple Locations, Russia
- Research Site, Multiple Locations, United Kingdom
Collaborators
Celgene Corporation
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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