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UnknownNCT05774340

A Study of CM326 in Subjects With Moderate to Severe Asthma

A Randomized, Double-Blind, Placebo-Controlled Phase Ⅱ Clinical Study to Evaluate the Efficacy and Safety of CM326 in Subjects With Moderate to Severe Asthma

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
207 (estimated)
Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is a multi-center, randomized, double-blind, placebo-controlled Phase Ⅱ 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 treatment period, and a 12-week safety follow-up period.

Conditions

Interventions

TypeNameDescription
DRUGCM326CM326 injection
OTHERPlaceboPlacebo

Timeline

Start date
2023-05-18
Primary completion
2025-01-01
Completion
2025-01-01
First posted
2023-03-17
Last updated
2023-12-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05774340. Inclusion in this directory is not an endorsement.

A Study of CM326 in Subjects With Moderate to Severe Asthma (NCT05774340) · Clinical Trials Directory