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Clinical Trial Summary

This was a multicenter, randomized, double-blind, placebo-parallel-controlled Phase II clinical study to evaluate the efficacy and safety of HRS9531 Injection compared to placebo in obese subjects with heart failure with preserved ejection fraction. A total of 200 obese subjects with heart failure with preserved ejection fraction would be enrolled. Eligible subjects were randomly assigned to either HRS9531 group or placebo group and were treated with HRS9531 injection or placebo, respectively, for 52 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06391710
Study type Interventional
Source Fujian Shengdi Pharmaceutical Co., Ltd.
Contact Zhou Li
Phone +86 17721288193
Email zhou.li.zl69@hengrui.com
Status Not yet recruiting
Phase Phase 2
Start date May 2024
Completion date January 2026

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