A Phase III Study of CM326 in Subjects With Moderate to Severe Asthma
A Randomized, Double-Blind, Placebo-Controlled Phase Ⅲ Clinical Study of Evaluating the Efficacy and Safety of CM326 in Subjects With Moderate to Severe Asthma
CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
230 participants
Jan 23, 2026
INTERVENTIONAL
Conditions
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.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
subcutaneous injection
subcutaneous injection
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07372287