CompletedPHASE1, PHASE2NCT00306969
Study of Oral Bexarotene in Combination With Photopheresis for 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
- Boston University
- Principal Investigator
- Marie-France Demierre, MDBoston University
- Intervention
- bexarotene(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2001 – 2004
Study locations (1)
- Boston University Medical Center, Boston, Massachusetts, United States
Collaborators
Ligand Pharmaceuticals
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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