Non-Segmental Facial Vitiligo Research Trial (30 Weeks)

Adults (male or female) ages 18 years and older with a clinical diagnosis of non-segmental vitiligo involving the face, may qualify to participate. Individuals can have vitiligo in other areas of the body, however the areas to be treated in the study will only include the face, neck, hands, forearms, and elbows. Vitiligo of the face involving at least 0.25% or more body surface area (BSA) involvement (i.e. one quarter of one handprint) is required; the maximum BSA permitted is 15%. Individuals must agree to discontinue all agents used to treat vitiligo from screening through the final safety follow-up visit.

Participants will receive investigational topical medication (active study drug) or placebo. Investigational medication and study-related care will be provided at no cost. A phototherapy unit (either active or sham) will be issued for home use. Reimbursement for study-related expenses may be provided.

Study participation will last about 30 weeks and involve about 9 visits to the study centre.

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Similar Studies

  • At this time there are no other studies for this condition. Please register to be contacted about upcoming studies for this condition.

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Why Take Part In a Clinical Study?

Regulatory agencies like Health Canada, Australia's Therapeutic Goods Administration and the FDA require that Clinical Research Trials be conducted in order to develop new treatments, preventions and devices for diseases or conditions. Clinical Research Trials are also referred to as Clinical Studies or Clinical Trials. read more