Clinical Trial

A Phase II Study of 9MW3811 in Patients With Pathological Scar

Recruiting Phase 2
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Summary
This is a randomized, double-blind, placebo-controlled Phase II study to evaluate the efficacy, safety, tolerability, pharmacokinetics, and immunogenicity of 9MW3811 in patients with pathological scar.
Trial Details
NCT Number NCT07576608
Lead Sponsor Mabwell (Shanghai) Bioscience Co., Ltd.
Conditions Scar
Enrollment 30 participants
Start Date 2025-12-29
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-05-08