U.S., Sept. 26 -- ClinicalTrials.gov registry received information related to the study (NCT07840820) titled 'Phase II/III Study of FXS5626 in Participants With Non-segmental Vitiligo' on Sept. 17.
Brief Summary: This is a multicenter, randomized, double-blind, placebo-controlled, adaptive seamless design, Phase II/III study evaluating the efficacy and safety of FXS5626 in participants with non-segmental vitiligo.
Study Start Date: Oct. 30
Study Type: INTERVENTIONAL
Condition:
Non-segmental Vitiligo
Intervention:
DRUG: Intervention1: FXS5626 Tablets
FXS5626 tablets administered orally twice daily (BID) for 24 weeks.
DRUG: Intervention2: FXS5626 Tablets
FXS5626 tablets administered orally twice daily (BID) for 24 weeks.
DRUG: Inte...