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Clinical Trial Summary

The aim of the study is to evaluate the efficacy and safety of XW003 versus placebo in adults with overweight or obesity


Clinical Trial Description

In this Phase 3 study, eligible participants will be randomized into three cohorts in a 3:1:3:1:3:1 ratio to receive once-weekly subcutaneous XW003 (low, medium, or high dosage) or volume-matching placebo for 48 weeks, including a dose-escalation period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05813795
Study type Interventional
Source Hangzhou Sciwind Biosciences Co., Ltd.
Contact
Status Active, not recruiting
Phase Phase 3
Start date April 5, 2023
Completion date January 22, 2025

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