CompletedPhase 2NCT00030849
Bexarotene and Interferon Alfa in Treating Patients With Cutaneous T-Cell Lymphoma
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
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- David J. Straus, MDMemorial Sloan Kettering Cancer Center
- Intervention
- recombinant interferon alfa(biological)
- Eligibility
- 18 years · All sexes
- Timeline
- 2001 – 2009
Study locations (5)
- University of Miami Sylvester Comprehensive Cancer Center, Miami, Florida, United States
- NYU School of Medicine's Kaplan Comprehensive Cancer Center, New York, New York, United States
- Memorial Sloan-Kettering Cancer Center, New York, New York, United States
- Abramson Cancer Center of the University of Pennsylvania Medical Center, Philadelphia, Pennsylvania, United States
- University of Texas - MD Anderson Cancer Center, Houston, Texas, United States
Collaborators
National Cancer Institute (NCI)
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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