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LY4005130 antibody treatment for nonsegmental vitiligo
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
Status: Recruiting now
Description:
Eli Lilly and Company plans to enroll about 66 participants. LY4005130 is an experimental antibody that neutralizes XCL1 and XCL2 signals linked to harmful CD8 T cells. It is designed to reduce the immune attack on melanocytes and encourage repigmentation. Possible risks include infusion reactions, headache, and infections; its full safety profile is not yet known. People ages 18 to 75 may qualify. The study is recruiting at 35 listed sites across 5 countries.
Start date: April 14, 2026
Completion date: September 01, 2027
Organizer: Eli Lilly and Company
Contact: Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
Tel.: 1-317-615-4559
Email: LillyTrials@Lilly.com
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FAQOther Questions
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Localized vitiligo, where the white patches are limited to one or a few areas of the body, can be managed with a few treatment approaches. The best therapy usually depends on th...
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In 2016, the United Nations marked World Vitiligo Day in its International Calendar of Disability Events. However, it was removed in 2019 when the calendar was streamlined to 'M...
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