Condition: Moderate to Severe Asthma · Sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
This study is a multi-center, randomized, double-blind, placebo-controlled Phase Ⅱ/Ⅲ 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 52-week randomized treatment period, and a 4-week safety follow-up period.
This description comes directly from the study's public registry record.
Wang Wenjuan · 010-63942533 · wangwenjuan01@cspc.cn
Always discuss trial participation with your own doctor first.
| China-Japan Friendship Hospital | Beijing, Beijin, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05761028