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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 atopic dermatitis.


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 NCT05544591
Study type Interventional
Source Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date October 26, 2022
Completion date September 20, 2023

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