drugset / Trial / NCT05186909

A Study of CM310 in Subjects With Moderate to Severe Asthma

NCT05186909

Phase 2 Completed 52 enrolled Keymed Biosciences Co.Ltd
RandomizedParallel-groupQuadruple-blindTreatment

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 CM310 in subjects with moderate to severe asthma. The study consists of three periods, including an up to 4-week screening period, a 24-week randomized treatment period, and a 8-week safety follow-up period.

Timeline

Start
2022-01-12
Primary completion
2023-09-13
Completion
2023-09-13

Drugs

EvaluationDrugModalityDoseRoute
Subject CM310 Monoclonal antibody 150 mg Subcutaneous
Subject CM310 Monoclonal antibody 300 mg Subcutaneous

Indications