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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT04818346

Public ClinicalTrials.gov record NCT04818346. 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 21, 2026, 5:27 PM 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 Followed by an Extension Period in Participants With Vitiligo

Study identification

NCT ID
NCT04818346
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
171 participants

Conditions and interventions

Interventions

  • INCB054707 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
May 5, 2021
Primary completion
May 23, 2022
Completion
May 23, 2023
Last update posted
Apr 10, 2024

2021 – 2023

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Investigative Site 010 Hoover Alabama 35244
Investigative Site 015 Gilbert Arizona 85295
Investigative Site 028 Scottsdale Arizona 85260
Investigative Site 006 Irvine California 92697
Investigative Site 009 Los Angeles California 90036
Investigative Site 018 Los Angeles California 90045
Investigative Site 017 Sacramento California 95815
Investigative Site 032 Orange Park Florida 32073
Investigative Site 005 Tampa Florida 33613
Investigative Site 022 Tampa Florida 33614
Investigative Site 011 West Palm Beach Florida 33401
Investigative Site 024 Covington Louisiana 70433
Investigative Site 002 Brighton Massachusetts 02135
Investigative Site 023 Saint Paul Minnesota 55112
Investigative Site 027 Verona New Jersey 07044
Investigative Site 003 Columbus Ohio 43215
Investigative Site 007 Norman Oklahoma 73071
Investigative Site 001 Portland Oregon 97223
Investigative Site 021 Plymouth Meeting Pennsylvania 19462
Investigative Site 004 Murfreesboro Tennessee 37130
Investigative Site 033 Dallas Texas 75230
Investigative Site 012 San Antonio Texas 78213
Investigative Site 030 Spokane Washington 99202

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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04818346, 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 Apr 10, 2024 · Synced Jul 21, 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 NCT04818346 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →