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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of INCB054707 in Participants With Prurigo Nodularis

ClinicalTrials.gov ID: NCT05061693

Public ClinicalTrials.gov record NCT05061693. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 4:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study of the Efficacy and Safety of INCB054707 in Participants With Prurigo Nodularis

Study identification

NCT ID
NCT05061693
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
146 participants

Conditions and interventions

Interventions

  • INCB054707 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 3, 2021
Primary completion
Aug 10, 2023
Completion
Feb 27, 2024
Last update posted
Jul 10, 2025

2021 – 2024

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
22
Facility City State ZIP Site status
Investigative Site US010 Phoenix Arizona 85006
Investigative Site US024 Phoenix Arizona 85018
Investigative Site US001 Fountain Valley California 92708
Investigative Site US014 Sacramento California 95816
Investigative Site US019 Fort Lauderdale Florida 33308
Investigative Site US016 Miami Florida 33175
Investigative Site US013 Miramar Florida 33027
Investigative Site US009 Tampa Florida 33609-2231
Investigative Site 1071320 Newnan Georgia 30263
Investigative Site US008 Plainfield Indiana 46168
Investigative Site US011 South Bend Indiana 46617
Investigative Site US003 Baltimore Maryland 21287
Investigative Site US017 Troy Michigan 48084
Investigative Site US006 Saint Joseph Missouri 64506
Investigative Site US004 Portsmouth New Hampshire 03801
Investigative Site US023 Athens Ohio 45701
Investigative Site US002 Dublin Ohio 43016
Investigative Site US012 Gahanna Ohio 43230
Investigative Site US022 Murfreesboro Tennessee 37130
Investigative Site US021 Arlington Texas 76011
Investigative Site US005 Austin Texas 78745
Investigative Site US018 Dallas Texas 75231
Investigative Site US007 Houston Texas 77004

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05061693, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05061693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →