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Study identifier: NCT06516952 Synced from ClinicalTrials.gov · August 03, 2026
● Active Not Recruiting

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

Condition: Prurigo Nodularis  ·  Sponsor: Incyte Corporation

PhasePhase 3
Planned participants349
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (120)

Cahaba DermatologyBirmingham, Alabama, United States
Banner - University Medicine Multispecialty Services ClinicTucson, Arizona, United States
Premier Dermatology Clinical Trials Institute At Northwest ArkansasFayetteville, Arkansas, United States
Burke Pharmaceutical ResearchHot Springs, Arkansas, United States
Dermatology Research AssociatesLos Angeles, California, United States
NorthridgeNorthridge, California, United States
Rendon Center the Dermatology and Aesthetic CenterBoca Raton, Florida, United States
Driven Research LlcCoral Gables, Florida, United States
University of Miami Miller School of MedicineMiami, Florida, United States
Research Institute of the Southeast, LlcWest Palm Beach, Florida, United States
Illinois Dermatology Institute the Chicago LoopChicago, Illinois, United States
Chicago Cosmetic Surgery and DermatologyChicago, Illinois, United States

+ 108 more locations — full list on the registry record.

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