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This study will evaluate the efficacy, tolerability and safety of the topical application of mechlorethamine (MCH) formulations in patients with stage I or IIA mycosis fungoides (MF).
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Lead Sponsor
Yaupon Therapeutics
NCT05414500 · Cutaneous T Cell Lymphoma, Mycosis Fungoides
NCT06207812 · Lymphomatoid Papulosis, Mycosis Fungoides
NCT06588868 · Cutaneous T Cell Lymphoma, Cutaneous T-Cell Lymphoma/Mycosis Fungoides, and more
NCT06716658 · Lymphoma, T-Cell, NK-LGL Leukemia, and more
NCT06470451 · CTCL/ Mycosis Fungoides, CTCL, and more
Stanford University Medical Center
Stanford, California
Northwestern University - Dept. of Dermatology
Chicago, Illinois
NYU Medical Center Dept. of Dermatology
New York, New York
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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