Premier Clinical Research | Spokane, WA
Status and phase
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About
This study is being conducted to determine the efficacy and safety of povorcitinib in participants with nonsegmental vitiligo.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Aged ≥ 18 years.
Clinical diagnosis of nonsegmental vitiligo and meet the following:
Agreement to discontinue all agents and procedures used to treat vitiligo from screening through the final safety follow-up visit.
Willingness to avoid pregnancy or fathering children.
Exclusion criteria
Other protocol-defined Inclusion/Exclusion Criteria may apply.
Primary purpose
Allocation
Interventional model
Masking
444 participants in 2 patient groups, including a placebo group
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Central trial contact
Incyte Corporation Call Center (US); Incyte Corporation Call Center (ex-US)
Data sourced from clinicaltrials.gov
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