A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN2)
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Incyte Corporation
- Study ID
- NCT06516965
- 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
- Apr 2026
- Primary completion
- Oct 19, 2026
- Completion
- May 3, 2027
Study Design
- Enrollment
- 346 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 (28)
Find similar trials in Phoenix, AZ
By research site
Medical Dermatology Specialists Phoenix· Phoenix, AZInvestigate Md· Scottsdale, AZFirst Oc Dermatology Research Inc· Fountain Valley, CAClinical Science Institute Clinical Research Specialists Inc· Santa Monica, CACenter For Clinical and Cosmetic Research· Aventura, FLSchweiger Dermatology· Boca Raton, FL
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