Huashan Hospital, Fudan University, Shanghai, Shanghai Municipality, China (Recruiting) - 18 Apr `26IBI3013 or baricitinib for nonsegmental vitiligo

IBI3013 or baricitinib for nonsegmental vitiligo

Official title: Evaluation of the Safety, Tolerability, and Pharmacokinetics of Single-dose Administration of IBI3013 in Healthy Adult Trial Participants and Multiple-dose Administration in Active Non-segmental Vitiligo Trial Participants and Severe Alopecia Areata Trial Participants - a Randomized, Double-blind, Placebo-controlled, Dose-escalation Study

Status: Recruiting now

Description:

Innovent Biologics (Suzhou) Co. Ltd. plans to enroll about 160 participants. The experimental antibody blocks IL-15, an immune signal that helps pigment-destroying T cells survive. Researchers hope it will reduce the immune attack on melanocytes and allow skin color to return. Possible risks include injection or infusion reactions, headache, and infections; longer-term risks are still being studied. People ages 18 to 80 may qualify. The study is recruiting at one listed site in China.

Start date: April 18, 2026

Completion date: December 31, 2028

Organizer: Innovent Biologics (Suzhou) Co. Ltd.

Contact: juan chen

Tel.: 021 3183 7200

Email: juan.chen01@innoventbio.com

Link: https://clinicaltrials.gov/study/NCT07554222

Clinical Trial Alerts

Sign up and be the first to know about updates on this trial.

This request will be sent with the trial reference IBI3013 or baricitinib for nonsegmental vitiligo . By submitting you agree to our Privacy Policy.

FAQOther Questions