A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2
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.
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
- 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
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 public registry record, listed eligibility criteria, and available contact information for NCT06072183 live on ClinicalTrials.gov.