Clinical Trial

Recombinant Anti-human IL-17A/F Humanized Monoclonal Antibody Injection in the Treatment of Moderate-to-Severe Active AS

Completed Phase 3
View on ClinicalTrials.gov →
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.
Trial Details
NCT Number NCT07498634
Lead Sponsor Zhejiang Kanova Biopharmaceutical Co., LTD
Conditions Phase III
Enrollment 323 participants
Start Date 2023-09-21
Primary Completion 2025-08-01 (estimated)
Study Completion 2025-11-14 (estimated)
Updated on ClinicalTrials.gov 2026-03-27