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RECRUITING
NCT07431177
PHASE2

A Phase IIb Dose-ranging Study to Assess the Efficacy and Safety of GIA632 in Participants With Non-segmental Vitiligo

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

Summary

The main purpose of this multicenter, randomized, double-blind, placebo-controlled Phase 2b study is to investigate the safety and efficacy of GIA632 in participants with NSV and to identify the optimal dose to be promoted into the confirmatory Phase 3 program.

Official title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-ranging Phase IIb Study to Assess the Efficacy and Safety of GIA632 in Adult Participants With Non-segmental Vitiligo Followed by an Extension Period

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

210

Start Date

2026-03-09

Completion Date

2030-01-28

Last Updated

2026-05-27

Healthy Volunteers

No

Interventions

DRUG

GIA632

GIA632 will be administered during the 48-week core period.

DRUG

Placebo

Placebo will be administered during the 48-week core period.

Locations (26)

Cahaba Derm and skin hlth ctr 27

Birmingham, Alabama, United States

MedDerm Associates

San Diego, California, United States

Clinical Trials Research Institute

Thousand Oaks, California, United States

Miami Derm and Laser Institute

Miami, Florida, United States

Global Clinical Professionals

St. Petersburg, Florida, United States

Dawes Fretzin Clinical Rea Group

Indianapolis, Indiana, United States

Hamzavi Dermatology

Fort Gratiot, Michigan, United States

Revival Research Institute

Troy, Michigan, United States

Skin Specialists PC

Omaha, Nebraska, United States

Las Vegas Dermatology

Las Vegas, Nevada, United States

Equity Medical

The Bronx, New York, United States

International Clinical Research Tennessee LCC

Murfreesboro, Tennessee, United States

Center for Clinical Studies

Houston, Texas, United States

Austin Inst for Clinical Research

Pflugerville, Texas, United States

ACRC Trials

Plano, Texas, United States

Virginia Clinical Research

Norfolk, Virginia, United States

Novartis Investigative Site

Sydney, New South Wales, Australia

Novartis Investigative Site

Waitara, New South Wales, Australia

Novartis Investigative Site

Melbourne, Victoria, Australia

Novartis Investigative Site

Mississauga, Ontario, Canada

Novartis Investigative Site

Newmarket, Ontario, Canada

Novartis Investigative Site

Toronto, Ontario, Canada

Novartis Investigative Site

Québec, Quebec, Canada

Novartis Investigative Site

Shanghai, China

Novartis Investigative Site

Urayasu, Chiba, Japan

Novartis Investigative Site

Kofu, Yamanashi, Japan