INCB54707-305 Enrolling

Prurigo Nodularis Study (13 Months)


Treatment: Oral Age: 18 to 75 Years


Who Can Participate?

Adults (18-75) with prurigo nodularis (PN) may participate.

Inclusion Criteria

  • have a clinical diagnosis of PN for at least 3 months
  • 20 or more pruriginous lesions in total on 2 or more different body regions (both legs, and/or both arms, and/or trunk)

General Information

  • No cost to participate or receive study treatment
  • Regular visits with study doctors who specialise in treating PN (15 visits)
  • Reimbursement for study-related expenses may be provided

How Long Will The Study Last?

  • 56 weeks

Participating Locations

COUNTRY
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United States
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Canada

Participating Experts

No Doctors Found

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The following information is from ClinicalTrials.gov

Last Update Posted: April 15, 2025

Official Title

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis

ClinicalTrials.gov ID

NCT06516952

Sponsor

Incyte Corporation

Study Description

  • Brief Summary:

    The purpose of this study is to evaluate effect of povorcitinib on itch and skin lesions in participants with prurigo nodularis.

  • Condition or Disease:

    Prurigo Nodularis

  • Intervention/Treatment:

    Drug: Povorcitinib Drug: Povorcitinib Drug: Placebo
  • Phase:

    PHASE 3

  • Ages Eligible for Study:

    18 Years to 75 Years (ADULT,OLDER_ADULT)

  • Sexes Eligible for Study:

    ALL


Terms and Conditions – ClinicalTrials.gov
Purpose of ClinicalTrials.gov Database. The U.S. National Institutes of Health, Department of Health and Human Services, through its National Library of Medicine, has developed ClinicalTrials.gov to provide patients, family members, and members of the public current information about clinical research studies.



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Prurigo Nodularis

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