Combining Topical Imiquimod With Local Radiotherapy for Treatment of Mycosis Fungoides

Recruiting Early Phase 1 Interventional Study
Mycosis Fungoides
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 90
Sex
Any
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
25 (estimated)
Sponsor
Northwestern University · Other
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About This Trial
Mycosis fungoides (MF) is the most common subtype of cutaneous T cell lymphoma (MF) and presents as cutaneous patches, plaques, and tumors. Radiation therapy (RT) is a frequently pursued management option for CTCL, especially in patients with more advanced skin disease. Imiquimod stimulates a Th1 lymphocyte response with increased IL-2 and IFN-α, but also induces IFN-α, TNF-α, IL-1α, IL-6, and IL-…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients must have confirmed stage IA-IIB mycosis fungoides. * Patients must be 18-90 years of age. * Patients must have failed at least one standard therapy for MF. * Patients must have active, but stable disease for \>6 months. * Patients must have 4 or more discrete MF lesi…
Contacts

Dermatology Clinical Trials Unit

312-503-5944

NUderm-research@northwestern.edu

CONTACT