CompletedNCT02296164

Clinical Study Assessing Outcomes, Adverse Events, Treatment Patterns, and Quality of Life in Patients Diagnosed With Mycosis Fungoides Cutaneous T-cell Lymphoma

Studying Aggressive primary cutaneous T-cell lymphoma

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Helsinn Therapeutics (U.S.), Inc
Principal Investigator
Bill Bailey
Helsinn Therapeutics (U.S.), Inc
Intervention
Valchlor(drug)
Enrollment
300 enrolled
Eligibility
18 years · All sexes
Timeline
20142018

Study locations (30)

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 NCT02296164 on ClinicalTrials.gov

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