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Clinical Trial Summary

The primary objective of the study was to evaluate the efficacy and safety of 611 in Chinese adults with moderate to severe COPD.


Clinical Trial Description

The maximum study duration was 28 weeks per participants, including a screening period of up to 4 weeks, a 16-week randomized treatment period, and a 8-week follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06099652
Study type Interventional
Source Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
Contact Qinghong Zhou, BS
Phone +86 18911301578
Email zhouqinghong@3sbio.com
Status Recruiting
Phase Phase 2
Start date December 8, 2023
Completion date May 2025

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