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A Study of LY4005130 in Adult Participants With Non-Segmental Vitiligo
Sponsor: Eli Lilly and Company
Summary
The purpose of this study is to evaluate how well LY4005130 is tolerated and what side effects may occur in participants with non-segmental vitiligo (NSV) when compared with placebo. The study drug will be administered intravenously (IV) (into a vein in the arm). Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. The study will last approximately 48 weeks, including screening.
Official title: A Phase 2, Randomized, 24-Week, Multicenter, Double-Blind, Placebo-Controlled Proof-of-Concept Study to Investigate Efficacy and Safety of LY4005130 in Adult Participants With Non-Segmental Vitiligo
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2026-04-14
Completion Date
2027-09
Last Updated
2026-04-27
Healthy Volunteers
No
Conditions
Interventions
LY4005130
Administered IV
Placebo
Administered IV
Locations (35)
Medical Dermatology Specialists
Phoenix, Arizona, United States
Saguaro Dermatology - Phoenix
Phoenix, Arizona, United States
Center For Dermatology Clinical Research, Inc.
Fremont, California, United States
Northridge Clinical Trials
Northridge, California, United States
Cura Clinical Research - Oxnard
Oxnard, California, United States
Cura Clinical Research - Santa Clarita - Kelly Johnson Parkway
Santa Clarita, California, United States
Health Clinical Research, LLC
Miami, Florida, United States
K2 Medical Research - Tampa
Tampa, Florida, United States
Advanced Medical Research, PC.
Sandy Springs, Georgia, United States
Dawes Fretzin Clinical Research Group, LLC
Indianapolis, Indiana, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Revival Research Institute, LLC
Troy, Michigan, United States
Stracskin
Portsmouth, New Hampshire, United States
Equity Medical
The Bronx, New York, United States
Accurate Clinical Research, Inc
Humble, Texas, United States
Texas Dermatology and Laser Specialists - San Antonio - South New Braunfels Avenue
San Antonio, Texas, United States
Jordan Valley Dermatology & Research Center
South Jordan, Utah, United States
Clinical Research Partners, LLC
Richmond, Virginia, United States
ANIMA Research
Alken, Belgium
UZ Gent
Ghent, Belgium
Centre Hospitalier Universitaire de Liège - Domaine Universitaire du Sart Tilman
Liège, Belgium
INTERMED Groupe Sante
Chicoutimi, Canada
DermEffects
London, Canada
Dar Clinical Research - Ottawa - Hunt Club Road
Ottawa, Canada
The Centre for Dermatology
Richmond Hill, Canada
Research Toronto
Toronto, Canada
SIMa Recherche
Verdun, Canada
Peking University People's Hospital
Beijing, China
Hangzhou Third People's Hospital
Hangzhou, China
Shanghai Skin Disease Hospital
Shanghai, China
The University of Hong Kong-Shenzhen Hospital
Shenzhen, China
Centrum Badan Klinicznych PI-House sp. z o.o.
Gdansk, Poland
Diamond Clinic
Krakow, Poland
Dermedic Jacek Zdybski
Ostrowiec Świętokrzyski, Poland
Centrum Medyczne Ginemedica
Wroclaw, Poland