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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Povorcitinib

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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