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Study identifier: NCT07144098 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Study of Pharmacokinetics and Safety of GZR18 Injection in Subjects With Liver Insufficiency and Normal Liver Function

Condition: Obesity/Overweight  ·  Sponsor: Gan & Lee Pharmaceuticals.

PhasePhase 1
Planned participants24
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

This study adopts a multicenter, single-dose, open-label, and parallel design, which is aimed at assessing the PK and safety profiles of GZR18 Injection in subjects with normal liver function and those with mild, moderate or severe liver insufficiency. The study duration for each subject in this study is up to 50 days, including a screening period of up to 14 days (Day-14 to Day-1), an 8-day dosing/observation period (Day 1 to Day 8), and a 28-day follow-up period (Day 9 to Day 36).

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

Talk to the study team

Li yuan Zhao, Ph.D  ·  010-8059-5000  ·  liyuan.zhao@ganlee.com

Always discuss trial participation with your own doctor first.

Locations (1)

Gan & Lee PharmaceuticalsBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07144098