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Study identifier: NCT07150962 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Recruiting

Relative Bioavailability of First vs Second-Generation Formulations of HRS9531 Tablets in Obese or Overweight Subjects

Condition: Overweight or Obesity  ·  Sponsor: Fujian Shengdi Pharmaceutical Co., Ltd.

PhasePhase 1
Planned participants168
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersNo

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About this study

This study aims to compare the relative bioavailability, safety and tolerability of the first-generation and second-generation formulations of HRS9531 tablets, as well as to explore the safety, tolerability and pharmacokinetic characteristics of the second-generation formulation in terms of single-dose escalation.

This description comes directly from the study's public registry record.

Talk to the study team

Jingjing Wang  ·  +86-0518-82342973  ·  jingjing.wang@hengrui.com

Tong Zhang  ·  +86-0518-82342973  ·  tong.zhang.tz58@hengrui.com

Always discuss trial participation with your own doctor first.

Locations (1)

The Second Affiliated Hospital of Anhui Medical UniversityHefei, Anhui, ChinaRecruiting

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