CompletedPhase 1NCT00554827
Study of Pralatrexate in Patients With Relapsed or 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
- Acrotech Biopharma Inc.
- Principal Investigator
- Michael Saunders, MDSpectrum Pharmaceuticals, Inc
- Intervention
- Vitamin B12(dietary_supplement)
- Enrollment
- 55 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2007 – 2012
Study locations (10)
- City of Hope National Medical Center, Duarte, California, United States
- Stanford University School of Medicine, Redwood City, California, United States
- Yale University School of Medicine, New Haven, Connecticut, United States
- Emory University, Atlanta, Georgia, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- Memorial Sloan-Kettering Cancer Center, New York, New York, United States
- Columbia University Medical Center, New York, New York, United States
- University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- Fred Hutchinson Cancer Center, Seattle, Washington, 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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