Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Povorcitinib clinical trials

Also listed in trial records as INCB054707, INCB54707
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 8 trials in our USA, Canada, Germany, Poland, France, Spain, UK, Italy, Netherlands, Belgium, Japan, Austria, Czechia, Australia, Mexico, Switzerland, South Korea and Denmark registers that name Povorcitinib as an intervention. Synced 9 Nov 2026
8Current trials
2Recruiting now
1Lead sponsor
18Country registers
At a glance

Povorcitinib is named as an intervention in 8 current clinical trials in our USA, Canada, Germany, Poland, France, Spain, UK, Italy, Netherlands, Belgium, Japan, Austria, Czechia, Australia, Mexico, Switzerland, South Korea and Denmark registers. 2 are recruiting patients now. The most common phase is Phase 3. The lead sponsor is Incyte Corporation. The most-studied condition is Hidradenitis Suppurativa (HS).

How Povorcitinib works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Hidradenitis suppurativaPhase 3
  • Prurigo nodularisPhase 3
  • VitiligoPhase 3
  • AsthmaPhase 2

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5095079, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 11881, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Povorcitinib

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting225%
  • Active, closed675%

Trials by phase

  • Phase 3675%
  • Phase 2225%
01

Clinical trials of Povorcitinib

8 trials
StudyPhaseStatusLead sponsorRegisters
Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib
NCT06855498 · Hidradenitis Suppurativa (HS)
Phase 3 Recruiting Incyte Corporation UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Switzerland, Austria, Czechia, Canada, South Korea, Australia
Pharmacokinetics, Safety, and Efficacy of Povorcitinib in Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa
NCT07213973 · Hidradenitis Suppurativa (HS)
Phase 2 Recruiting Incyte Corporation USA, Canada, Mexico
A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V1)
NCT06113445 · NonSegmental Vitiligo
Phase 3 Active, closed Incyte Corporation USA, Germany, France, Spain, Netherlands, Belgium, Poland, Canada, Mexico, Japan
A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)
NCT06113471 · NonSegmental Vitiligo
Phase 3 Active, closed Incyte Corporation UK, USA, Germany, France, Italy, Poland, Canada
A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa
NCT06212999 · Hidradenitis Suppurativa (HS)
Phase 3 Active, closed Incyte Corporation UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Denmark, Poland, Austria, Czechia, Canada, Japan, Australia
A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1)
NCT06516952 · ClinicalTrials.gov ↗ · Prurigo Nodularis
Phase 3 Active, closed Incyte Corporation USA, Germany, France, Italy, Netherlands, Poland, Switzerland, Austria, Canada, Mexico, South Korea
A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN2)
NCT06516965 · Prurigo Nodularis
Phase 3 Active, closed Incyte Corporation UK, USA, Germany, Spain, Belgium, Poland, Czechia, Canada, Japan, Australia
A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Inadequately Controlled Moderate to Severe Asthma
NCT05851443 · Moderate to Severe Asthma
Phase 2 Active, closed Incyte Corporation USA, Germany, Spain, Poland, Canada, Japan

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Povorcitinib

4 conditions
Hidradenitis Suppurativa (HS)3Prurigo Nodularis2NonSegmental Vitiligo2Moderate to Severe Asthma1
05

Related compounds

06

Questions about Povorcitinib trials

How many clinical trials are testing Povorcitinib?

8 current trials in our USA, Canada, Germany, Poland, France, Spain, UK, Italy, Netherlands, Belgium, Japan, Austria, Czechia, Australia, Mexico, Switzerland, South Korea and Denmark registers name Povorcitinib (also registered as INCB054707) as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are Povorcitinib trials recruiting patients?

Yes. 2 of the 8 trials are recruiting: 2 with sites in USA, 2 with sites in Canada, 1 with sites in Germany, 1 with sites in Poland, 1 with sites in France, 1 with sites in Spain, 1 with sites in UK, 1 with sites in Italy, 1 with sites in Netherlands, 1 with sites in Belgium, 1 with sites in Austria, 1 with sites in Czechia, 1 with sites in Australia, 1 with sites in Mexico, 1 with sites in Switzerland and 1 with sites in South Korea. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Povorcitinib clinical trials?

The lead sponsor is Incyte Corporation. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Povorcitinib works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Povorcitinib works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Povorcitinib (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.