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NCT06855498: STOP-LTR

Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib

Recruiting now Phase 3 Last updated 8 April 2026
What this trial tests

Phase 3 trial testing povorcitinib in Hidradenitis Suppurativa (HS) in 600 participants. Currently enrolling.

Timeline
28 February 2025
Primary endpoint
28 February 2028
28 February 2028

Quick facts

Lead sponsorIncyte Corporation
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment600
Start date28 February 2025
Primary completion28 February 2028
Estimated completion28 February 2028
Sites316 locations across Italy, Poland, South Korea, Denmark, Netherlands, Belgium, Bulgaria, United States

Drugs / interventions tested

Conditions studied

Sponsor

Incyte Corporation — full company profile →

Who can join

18 and older, any sex, with Hidradenitis Suppurativa (HS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Rollover study for participants from predetermined, Incyte-sponsored parent clinical trials of povorcitinib.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of povorcitinib

Trials testing the same drug.

Other recruiting trials for Hidradenitis Suppurativa (HS)

Currently open trials in the same condition.

Other Incyte Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06855498.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing