U.S., March 28 -- ClinicalTrials.gov registry received information related to the study (NCT07498634) titled 'Recombinant Anti-human IL-17A/F Humanized Monoclonal Antibody Injection in the Treatment of Moderate-to-Severe Active AS' on March 18.
Brief Summary: This is a multicenter, randomized, double-blind, placebo-controlled, and parallel grouping study.
Study procedures: The screening period does not exceed 4 weeks, including 16 weeks for initial treatment, 28 weeks for maintenance treatment and 8 weeks for safety follow-up.
Study Start Date: Sept. 21, 2023
Study Type: INTERVENTIONAL
Condition:
Phase III
Intervention:
DRUG: XKH004
Recombinant Anti-human IL-17A/F Humanized Monoclonal Antibody Injection
DRUG: Placebo
Placebo
Rec...