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Clinical Trial Summary

This study will assess the efficacy and safety of 610 as an adjunctive therapy in adult subjects with severe eosinophilic asthma.


Clinical Trial Description

This is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of 610 in adults with severe eosinophilic asthma. Plan to recruit 120 subjects, and the subjects divided into 3 groups: 610 100mg group, 610 300mg group and placebo group. The study is divided into screening period of 4 weeks, treatment period of 16 weeks and follow-up period of 8 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05528679
Study type Interventional
Source Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
Contact Qinghong Zhou, MD
Phone 18911301578
Email zhouqinghong@3sbio.com
Status Not yet recruiting
Phase Phase 2
Start date September 2022
Completion date September 2023

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