CompletedPhase 2NCT00535470
An Open Label Study to Evaluate the Safety and Efficacy of Mechlorethamine(MCH) 0.04% Formulation in Mycosis Fungoides
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
- Yaupon Therapeutics
- Principal Investigator
- Stuart Lessin, M.D., Pharm.DFox Chase Cancer Center
- Intervention
- 0.04% Mechlorethamine gel(drug)
- Enrollment
- 100 enrolled
- Eligibility
- All sexes
- Timeline
- 2007 – 2011
Study locations (11)
- Stanford University Medical Center, Stanford, California, United States
- Northwestern University-Dept. of Dermatology, Chicago, Illinois, United States
- Columbia University, Dept of Dermatology, New York, New York, United States
- NYU Medical Center Dept. of Dermatology, New York, New York, United States
- Duke University Medical Center, Durham, North Carolina, United States
- Oklahoma University, Tulsa, Oklahoma, United States
- Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
- University of Texas, Southwestern Medical Center, Dallas, Texas, United States
- The University of Texas, M.D. Anderson Cancer Center, Houston, Texas, United States
- Utah Clinical Trials, LLC, Salt Lake City, Utah, United States
- University of Wisconsin, Madison, Wisconsin, 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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