CompletedPHASE1, PHASE2NCT00061880
BCX-1777 in Treating Patients With Refractory 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
- Alex Shalaurov, MD, PhD, M.DInveresk Research Group, Incorporated
- Intervention
- forodesine hydrochloride(drug)
- Eligibility
- 18 years · All sexes
- Timeline
- 2003 – 2008
Study locations (3)
- University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama, United States
- Duke Comprehensive Cancer Center, Durham, North Carolina, United States
- University of Texas - MD Anderson Cancer Center, Houston, Texas, United States
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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