Clinical Trial

Study of Stapokibart Injection in Subjects With Moderate to Severe Bullous Pemphigoid

Not Yet Recruiting Phase 3
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Summary
This study is a multicenter, randomized, double-blind, placebo-controlled phase III clinical study to evaluate the efficacy, safety, pharmacokinetics, pharmacodynamics, and immunogenicity of Stapokibart in subjects with Moderate to Severe Bullous Pemphigoid.
Trial Details
NCT Number NCT07210554
Lead Sponsor Chengdu Kangnuoxing Biopharma,Inc.
Conditions Bullous Pemphigoid (BP)
Enrollment 200 participants
Start Date 2025-11-11
Primary Completion 2028-03-27 (estimated)
Study Completion 2028-05-08 (estimated)
Updated on ClinicalTrials.gov 2025-10-07