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Search / Trial NCT06163326

A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental Vitiligo

Launched by PFIZER · Nov 30, 2023

Trial Information

Current as of August 22, 2025

Recruiting

Keywords

Stable Vitiligo Active Vitiligo Adults Adolescents

ClinConnect Summary

This clinical trial is studying a medication called ritlecitinib to see how safe and effective it is for people with non-segmental vitiligo, a skin condition that causes white patches due to a loss of pigment. The trial will explore if continuing ritlecitinib helps patients keep or improve their skin color recovery, or if starting a higher dose of ritlecitinib can lead to better results. Participants will take either ritlecitinib or a placebo (a pill with no active medication) for up to 52 weeks and will have regular check-ins to monitor their progress.

To join this study, participants need to be at least 12 years old, have non-segmental vitiligo, and have completed a previous study involving ritlecitinib or a placebo. During the trial, they will take the medication daily at home and attend up to nine visits to the study site for evaluations. This study aims to understand how ritlecitinib can help manage vitiligo better, contributing to potential improvements in treatment for this condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participants ≥18 years of age at Screening in Study B7981040. Adolescents (12 to \<18 years of age at Screening in the parent study) are also eligible for this study if approved by the local IRB/EC and regulatory health authority.
  • Participants who met the eligibility criteria and completed 52 weeks of study intervention for stable or active nonsegmental vitiligo in Study B7981040
  • The BL visit/first dose in Study B7981041 must be within 30 days after the week 52 visit in Study B7981040
  • Exclusion Criteria:
  • Participant met the parent study (Study 7981040) discontinuation criteria or discontinued the parent study for any safety-related event
  • Any active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation

About Pfizer

Pfizer Inc. is a global leader in biopharmaceutical innovation, dedicated to discovering, developing, and delivering advanced therapies that enhance patient outcomes across a wide range of medical conditions. With a rich history of scientific research and a commitment to quality, Pfizer focuses on areas such as oncology, immunology, cardiology, and rare diseases. The company leverages cutting-edge technology and collaborates with healthcare professionals, regulatory bodies, and academic institutions to conduct rigorous clinical trials that ensure the safety and efficacy of its products. Pfizer's mission is to bring breakthroughs that change patients' lives, exemplifying its commitment to health and wellness worldwide.

Locations

Ann Arbor, Michigan, United States

Charleston, South Carolina, United States

Melbourne, Victoria, Australia

San Antonio, Texas, United States

Barcelona, , Spain

Sendai, Miyagi, Japan

Cordoba, , Spain

Shinjuku Ku, Tokyo, Japan

Indianapolis, Indiana, United States

Seoul, , Korea, Republic Of

Bunkyo Ku, Tokyo, Japan

Nagoya, Aichi, Japan

Quebec, , Canada

Cleveland, Ohio, United States

Shanghai, Shanghai, China

Bad Bentheim, Niedersachsen, Germany

Chapel Hill, North Carolina, United States

Madrid, , Spain

Seoul, , Korea, Republic Of

Dallas, Texas, United States

Fuzhou, Fujian, China

Brooklyn, New York, United States

Fuzhou, Fujian, China

Suwon, , Korea, Republic Of

Kofu, Yamanashi, Japan

Quebec, , Canada

Sendai Shi, Miyagi, Japan

Guangzhou, Guangdong, China

Kunming, Yunnan, China

Tokyo, , Japan

Encinitas, California, United States

London, , United Kingdom

Las Palmas De Gran Canaria, Las Palmas, Spain

Columbus, Ohio, United States

Münster, Nordrhein Westfalen, Germany

Monterrey, Nuevo León, Mexico

Tampa, Florida, United States

Huntington Beach, California, United States

Seoul, Other, Korea, Republic Of

Ostrowiec Swietokrzyski, , Poland

Suwon Si, , Korea, Republic Of

Veracruz, , Mexico

Los Angeles, California, United States

Wilmington, North Carolina, United States

Campbelltown, South Australia, Australia

Carlton, Victoria, Australia

Mississauga, Ontario, Canada

Sakai, Osaka, Japan

Rockville, Maryland, United States

Baton Rouge, Louisiana, United States

Osielsko, Kujawsko Pomorskie, Poland

Darlinghurst, New South Wales, Australia

Markham, Ontario, Canada

Seoul, Seoul Teukbyeolsi [Seoul], Korea, Republic Of

Cordoba, Andalucía, Spain

Red Deer, Alberta, Canada

Sakai City, Osaka, Japan

Houston, Texas, United States

Guangzhou, Guangdong, China

Calgary, Alberta, Canada

Columbus, Ohio, United States

Hollywood, Florida, United States

Warszawa, Mazowieckie, Poland

Sofia, , Bulgaria

Boynton Beach, Florida, United States

Barcelona, Catalunya [Cataluña], Spain

Albuquerque, New Mexico, United States

Mexico City, Distrito Federal, Mexico

Istanbul, , Turkey

Stara Zagora, , Bulgaria

Largo, Maryland, United States

Dupnitsa, Kyustendil, Bulgaria

Sofia, Sofia (Stolitsa), Bulgaria

Houston, Texas, United States

Toronto, Ontario, Canada

Suwon, Kyǒnggi Do, Korea, Republic Of

Suwon Si, Kyǒnggi Do, Korea, Republic Of

Chapel Hill, North Carolina, United States

Lodz, łódzkie, Poland

Szczecin, Zachodniopomorskie, Poland

Wuhan, Hubei, China

Stuttgart, Baden Württemberg, Germany

Shenyang, Liaoning, China

Monterrey, , Mexico

Wilmington, North Carolina, United States

Kayseri, , Turkey

East Melbourne, Victoria, Australia

Córdoba, , Spain

Sakai City, Osaka, Japan

Ostrowiec Swietokrzyski, świętokrzyskie, Poland

Veracruz, , Mexico

Guangzhou, Guangdong, China

Manisa, , Turkey

Quebec, , Canada

Stuttgart, , Germany

Lodz, , Poland

Istanbul Fatih, Istanbul, Turkey

Patients applied

0 patients applied

Trial Officials

Pfizer CT.gov Call Center

Study Director

Pfizer

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported