A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN2)
← catalyst calendarNCT06516965 · readout in 61 d
Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →.
Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
346actual
Sites
119
Countries
Australia, Belgium, Canada +8
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-10-10 | actual | When the study began enrolling |
| Primary completion | 2026-10-19 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-05-03 | estimated | The whole study's end, after follow-up |
| First posted | 2024-07-24 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-04-14 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Prurigo Nodularis
Interventions
- Drug: Povorcitinib — also filed as INCB054707
- Drug: Placebo
Primary outcome
what the primary-completion date above is the date OFProportion of participants achieving Itch NRS4 and IGA-CPG-S-TS at Week 24
measured Week 24
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