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Study details
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Povorcitinib Trial for Hidradenitis Suppurativa

Incyte Corporation
NCT IDNCT07213973ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

40

Study length

about 2.3 years

Ages

12–17

Locations

23 sites in AL, AZ, CT +14

About this study

Researchers are testing povorcitinib, a medication, in adolescents with moderate to severe hidradenitis suppurativa. The trial will last 832 days and evaluate the drug's safety and effectiveness.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Povorcitinib
PhasePhase 2
DrugPovorcitinib
Primary goalApparent clearance

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low10%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

kinase inhibitor

Endpoints

Primary: Apparent clearance, Proportion of participants with Treatment-Emergent Adverse Events (TEAEs), Terminal half-life

Secondary: Change from baseline in Children's Dermatology Life Quality Index (CDLQI) score at each visit, Mean change from baseline in abscess count at each visit, Mean change from baseline in draining tunnel count at each visit, Mean change from baseline in inflammatory nodule count at each visit, Mean percentage change from baseline in abscess count at each visit, Mean percentage change from baseline in draining tunnel count at each visit, Mean percentage change from baseline in inflammatory nodule count at each visit, Proportion of participants who achieve Skin Pain Numeric Rating Scale (NRS)30 among participants with baseline Skin Pain NRS score ≥ 3