Clinical Trial for Prurigo Nodularis (PN) – 56 Weeks

Adults aged 18 or over with a clinical diagnosis of prurigo nodularis (PN) for at least 3 months may qualify for this study. Eligible individuals must meet all inclusion criteria including having 6 or more pruriginous lesions on more than 2 different body areas. The total estimated impacted body surface area (BSA) must be 20% or less.

Participants will receive investigational topical treatment (active study drug) or placebo. Study treatment and study-related assessments will be provided at no cost. Reimbursement for study-related expenses may be provided.

Study participation will last approximately 56 weeks and involve about 12 visits to the study centre.

If interested, please contact our Research Coordinator  at 416-633-0001 x 4 or e-mail [email protected].

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