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

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
Yaupon Therapeutics
Principal Investigator
Stuart Lessin, M.D., Pharm.D
Fox Chase Cancer Center
Intervention
0.04% Mechlorethamine gel(drug)
Enrollment
100 enrolled
Eligibility
All sexes
Timeline
20072011

Study locations (11)

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.

Open NCT00535470 on ClinicalTrials.gov

Other trials for Aggressive primary cutaneous T-cell lymphoma

Additional recruiting or active studies for the same condition.

See all trials for Aggressive primary cutaneous T-cell lymphoma

← Back to all trials