CompletedPhase 2NCT00501735
Forodesine in the Treatment of 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
- BioCryst Pharmaceuticals
- Principal Investigator
- Nashat Gabrail, MDGabrail Cancer Center
- Intervention
- Forodesine 200 mg(drug)
- Enrollment
- 144 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2007 – 2011
Study locations (30)
- University of Alabama at Birmingham, Comprehensive Cancer Ctr, Birmingham, Alabama, United States
- Stanford University Medical Center, Stanford, California, United States
- Yale Cancer Center, New Haven, Connecticut, United States
- Moffitt Cancer Center, Tampa, Florida, United States
- Emory University, Atlanta, Georgia, United States
- LSU Health Sciences Center, Feist-Weiller Cancer Center, Shreveport, Louisiana, United States
- Boston Medical Center, Boston, Massachusetts, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- Hackensack University Medical Ctr, Hackensack, New Jersey, United States
- Upstate Medical University, Syracuse, New York, United States
- Duke University Medical Center, Durham, North Carolina, United States
- Wake Forest University Health Sceinces, Dept. of Dermatology, Winston-Salem, North Carolina, United States
- Gabrail Cancer Center, Canton, Ohio, United States
- University Hospitals Case Medical Center, Dept. of Dermatology, Cleveland, Ohio, United States
- Hospital at the University of Pennsylvania, Philadelphia, Pennsylvania, United States
- +15 more locations on ClinicalTrials.gov
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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