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NCT06516952 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1)

A Phase 3 study of Prurigo Nodularis, sponsored by Incyte Corporation.

Recruiting
Registry status
Phase 3
Development phase
330
Enrollment target
20
Study locations

NCT06516952 is a Phase 3 study of Prurigo Nodularis that is actively recruiting participants, run by Incyte Corporation. The registered enrollment target is 330 participants, above the 206-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (60% higher). The trial reports 20 study locations across 9 states.

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The verdict

NCT06516952, a Phase 3 study of Prurigo Nodularis, is actively recruiting participants, sponsored by Incyte Corporation.

RECRUITING
Registry status
Phase 3
Development phase
330 participants
Enrollment target
20
Study locations

Study Summary

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

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Povorcitinib

Study Locations (20)

Florida

  • Rendon Center the Dermatology and Aesthetic Center - Boca Raton
  • Driven Research Llc - Coral Gables
  • University of Miami Miller School of Medicine - Miami
  • Research Institute of the Southeast, Llc - West Palm Beach

Illinois

  • Illinois Dermatology Institute the Chicago Loop - Chicago
  • Chicago Cosmetic Surgery and Dermatology - Chicago
  • Center For Medical Dermatology and Immunology Research - Chicago
  • Northshore University Healthsystem - Skokie

Michigan

  • Oakland Hills Dermatology - Auburn Hills
  • Hamzavi Dermatology - Fort Gratiot
  • Somerset Skin Centre - Troy

Arkansas

  • Premier Dermatology Clinical Trials Institute At Northwest Arkansas - Fayetteville
  • Burke Pharmaceutical Research - Hot Springs

California

  • Dermatology Research Associates - Los Angeles
  • Northridge - Northridge

Missouri

  • Medisearch Clinical Trials - Saint Joseph
  • Washington University School of Medicine - St Louis

Alabama

  • Cahaba Dermatology - Birmingham

Arizona

  • Banner - University Medicine Multispecialty Services Clinic - Tucson

Trial Details

FieldValue
Enrollment Target 330 participants
Start Date 2024-10-10
Est. Completion 2027-05-03
Phase Phase 3

Sponsor

Incyte Corporation

239 total trials

What the Registry Record Tells You About NCT06516952

The ClinicalTrials.gov registry entry for NCT06516952 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 330 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 206-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (60% higher). The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prurigo Nodularis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06516952 reports 20 study locations spanning 9 distinct geographic areas - top geographies include Florida, Illinois, Michigan.

Frequently Asked Questions

What is clinical trial NCT06516952 about?

NCT06516952 is a clinical study titled "A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1)". The purpose of this study is to evaluate effect of povorcitinib on itch and skin lesions in participants with prurigo nodularis.

What is the current status of trial NCT06516952?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 330 participants. The study started on 2024-10-10. Estimated completion is 2027-05-03.

What conditions does trial NCT06516952 study?

This clinical trial studies the following conditions: Prurigo Nodularis.

What interventions are being tested in trial NCT06516952?

The interventions under investigation include: Placebo (DRUG), Povorcitinib (DRUG).

Who is sponsoring clinical trial NCT06516952?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06516952 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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