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Active, not recruiting Phase 3 Interventional

A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2

ClinicalTrials.gov ID: NCT06072183

Public ClinicalTrials.gov record NCT06072183. 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 Oct 19, 2026, 2:00 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 3 RANDOMIZED, DOUBLE-BLIND, 52-WEEK PLACEBO-CONTROLLED MULTI-CENTER STUDY WITH A DOUBLE-BLIND 52-WEEK EXTENSION PERIOD WITH RANDOMIZED DOSE UP/DOSE DOWN TITRATION INVESTIGATING THE EFFICACY, SAFETY, AND TOLERABILITY OF RITLECITINIB IN ADULT PARTICIPANTS WITH NONSEGMENTAL VITILIGO

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to learn about the safety and effects of the study medicine ritlecitinib for the possible treatment of nonsegmental vitiligo. Vitiligo causes white patches on your skin when the cells that give your skin color are destroyed. Nonsegmental means that it can affect both sides of the body such as both knees and both hands. Ritlecitinib has been tested in earlier clinical studies and has a favorable safety profile. At present there are no approved medications taken by mouth to treat nonsegmental vitiligo. This study is seeking participants who: * Are 18 years of age or older. * are confirmed to have nonsegmental vitiligo for at least 3 months. * Are willing to stop all other treatments that they may be taking for vitiligo. In this study participants will be chosen by chance, like drawing names out of a hat to receive 1 of 3 treatments: •Part I where two different amounts of ritlecitinib (50 mg and 100 mg) are taken once daily. It will be compared to placebo. Placebo is a dummy capsule. It doesn't have any medicine used in the study. Participants receiving placebo who have not responded to treatment after 52 weeks will be given 100 milligrams or 50 milligrams of ritlecitinib for the remaining 52 weeks of the study. • In Part II, participants will only receive 100 milligrams of ritlecitinib. About 1000 participants will take part in Part I and around 450 in Part II globally. The study will compare the experiences of people receiving ritlecitinib to those of the people who do not. This will help see if ritlecitinib is safe and effective. People in Part I will be in this study for about 26 months and people in Part II will be in this study for about 14 months. During the study, participants in part I will need to visit the study site at least 17 times. In part II, participants will visit at least 11 times. Participants will undergo various tests and procedures such as: * vitiligo rating, * physical examinations, * hearing tests, * blood tests, * x-ray, * ECG, * photographs of areas with vitiligo. Participants will be asked to complete questionnaires about their vitiligo.

Study identification

NCT ID
NCT06072183
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
1,571 participants

Conditions and interventions

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 8, 2023 (Actual)
Primary completion
Jul 30, 2027 (Estimated)
Completion
Jul 30, 2027 (Estimated)
Last update posted
Jun 24, 2026

2023 – 2027

United States locations

U.S. sites
68
U.S. states
21
U.S. cities
50
Facility City State ZIP Site status
Center for Dermatology and Plastic Surgery/CCT Research Scottsdale Arizona 85260 —
Dermatology Trial Associates Bryant Arkansas 72022 —
First OC Dermatology Research Inc Fountain Valley California 92708 —
Seaside Audiology Vertigo & Ear Specialists Huntington Beach California 92648 —
Wallace Medical Group, Inc Los Angeles California 90056 —
Kaiser Permanente Oakland California 94611 —
Cura Clinical Research - Oxnard Oxnard California 93030 —
Mission Dermatology Center Rancho Santa Margarita California 92688 —
Peninsula Research Associates Rolling Hills Estates California 90274 —
Integrative Skin Science and Research Sacramento California 95815 —
University of California San Diego - La Jolla San Diego California 92122 —
Wolverine Clinical Trials Santa Ana California 92706 —
Encore Medical Research of Boynton Beach Boynton Beach Florida 33436 —
FXM Clinical Research - Fort Lauderdale Fort Lauderdale Florida 33308 —
Direct Helpers Research Center Hialeah Florida 33012 —
Clever Medical Research Miami Florida 33126 —
Miami Dermatology and Laser Institute Miami Florida 33133 —
SouthCoast Research Center Miami Florida 33136 —
University of Miami Dermatology Clinical Trials Unit Miami Florida 33136 —
University of Miami Miami Florida 33136 —
Bio-Medical Research LLC Miami Florida 33144 —
New Horizon Research Center Miami Florida 33165 —
Skin Research of South Florida Miami Florida 33173 —
Well Pharma Medical Research, Corp. Miami Florida 33173 —
FXM Clinical Research - Miami Miami Florida 33175 —
Health and Life Research Institute Miami Florida 33176 —
University of Miami, Kendall Office Miami Florida 33176 —
Floridian Research Institute Llc Miami Florida 33179 —
Sanitas Research Miami Florida 33186 —
Wellness Clinical Research Miami Lakes Florida 33016 —
FXM Clinical Research - Miramar Miramar Florida 33027 —
GCP Research, Global Clinical professionals St. Petersburg Florida 33714 —
Advanced Clinical Research Institute Tampa Florida 33607 —
USF Health Tampa Florida 33612 —
Sidney P. Smith, MD, PC dba Georgia Skin & Cancer Clinic Savannah Georgia 31419 —
Endeavor Health Audiology -CHICAGO Chicago Illinois 60625 —
Endeavor Health Audiology -LAKE BLUFF Lake Bluff Illinois 60044 —
Endeavor Health Audiology-NORTHBROOK Northbrook Illinois 60062 —
Endeavor Health Audiology-SKOKIE Skokie Illinois 60076 —
Endeavor Health-Dermatology Clinical Trials Unit Skokie Illinois 60077 —
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46250 —
The South Bend Clinic, LLC South Bend Indiana 46617 —
Dermatology and Skin Cancer Specialists, LLC Rockville Maryland 20850 —
Oakland Hills Dermatology Auburn Hills Michigan 48326 —
CS Mott Center Detroit Michigan 48201 —
Wayne Health Detroit Michigan 48201 —
Henry Ford Medical Center - New Center One Detroit Michigan 48202 —
MediSearch Clinical Trials Saint Joseph Missouri 64506 —
Physician Research Collaboration, LLC Lincoln Nebraska 68516 —
University of New Mexico Health Sciences Center Albuquerque New Mexico 87102 —
OptiSkin Medical New York New York 10128 —
DermResearchCenter of New York, Inc. Stony Brook New York 11790 —
DJL Clinical Research, PLLC Charlotte North Carolina 28211 —
Darst Dermatology Charlotte North Carolina 28277 —
Bexley Dermatology Research Bexley Ohio 43209 —
Centricity Research Columbus Ohio Multispecialty Columbus Ohio 43213 —
Oregon Dermatology and Research Center Portland Oregon 97210 —
Dermatology Associates of Plymouth Meeting Plymouth Meeting Pennsylvania 19462 —
Medical University of South Carolina Charleston South Carolina 29425 —
Columbia Dermatology & Aesthetics Columbia South Carolina 29212 —
Palmetto Clinical Trial Services - Greenville Greenville South Carolina 29615 —
Center for Clinical Studies Houston Texas 77004 —
Austin Institute for Clinical Research Pflugerville Texas 78660 —
Complete Dermatology Sugar Land Texas 77479 —
The Woodlands Dermatology Associates, PA The Woodlands Texas 77380 —
University of Utah Murray Utah 84107 —
Springville Dermatology - Springville/CCT Research Springville Utah 84663 —
Eurofins Cosmetics CRL LLC Forest Virginia 24551 —

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 161 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06072183, 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 Jun 24, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06072183 live on ClinicalTrials.gov.

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