drugset / Trial / NCT07372287

A Phase III Study of CM326 in Subjects With Moderate to Severe Asthma

NCT07372287 ↗

Phase 3 Recruiting 230 enrolled CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a multi-center, randomized, double-blind, placebo-controlled Phase Ⅲ clinical study to evaluate the efficacy, safety, PK characteristics, PD effects and immunogenicity of CM326 in subjects with moderate to severe asthma. The study consists of three periods, including an up to 4-week screening period, a 52-week double-blind randomized treatment period, and a 12-week safety follow-up period.

Timeline

Start
2026-01-23
Primary completion
2028-12-31
Completion
2029-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject OCANKITUG Monoclonal antibody — Subcutaneous

Indications