A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1)
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Incyte Corporation
- Study ID
- NCT06516952
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
- Prurigo Nodularis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Povorcitinib — DRUGOral Tablet
- Placebo — DRUGOral Tablet
Study Details
The purpose of this study is to evaluate effect of povorcitinib on itch and skin lesions in participants with prurigo nodularis.
Key Dates
- Start date
- Oct 10, 2024
- Status verified
- May 2026
- Primary completion
- Oct 19, 2026
- Completion
- May 3, 2027
Study Design
- Enrollment
- 349 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Povorcitinib Dose 1Povorcitinib at the protocol-defined dose.
- Experimental: Povorcitinib Dose 2Povorcitinib at the protocol-defined dose.
- Placebo Comparator: PlaceboPlacebo at the protocol-defined dose.
Primary Outcome Measure
Proportion of participants achieving Itch NRS4 and IGA-CPG-S-TS at Week 24 [ Time Frame: Week 24 ]
Locations (31)
Find similar trials in Birmingham, AL
By research site
Cahaba Dermatology· Birmingham, ALBanner - University Medicine Multispecialty Services Clinic· Tucson, AZPremier Dermatology Clinical Trials Institute At Northwest Arkansas· Fayetteville, ARBurke Pharmaceutical Research· Hot Springs, ARDermatology Research Associates· Los Angeles, CANorthridge· Northridge, CA
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