Clinical Trial

A Phase 2 Study on the Safety and Efficacy of the Anti-BAFF-R Monoclonal Antibody, ESG206, in Patients With Systemic Lupus Erythematosus

Not Yet Recruiting Phase 2
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Summary
This is a multicenter, randomized, double-blind, placebo-controlled Phase II study designed to evaluate the efficacy and safety of ESG206 in participants with Systemic Lupus Erythematosus (SLE).
Trial Details
NCT Number NCT07760155
Lead Sponsor Shanghai Escugen Biotechnology Co., Ltd
Conditions Systemic Lupus Erythematosus (SLE)
Enrollment 40 participants
Start Date 2026-09-01
Primary Completion 2028-03-31 (estimated)
Study Completion 2028-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-08-12