LivingGLP1
Study S003366

A Multicenter, Single-Dose, Parallel-Group, Open-Label Pharmacokinetic Study of HDM1005 Injection in Participants With Impaired Renal Function and Healthy Participants

Registration

Registration
NCT07559240
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
30
Start
2026-05-15
Primary completion
2026-06-12
Lead sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Conditions
Overweight; Obese
Interventions
DRUG:HDM1005
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Maximum Concentration (Cmax) [Up to Day 29]
  • Area Under the Concentration Time Curve From Time Zero to t [ AUC(0- t)] [Up to Day 29]

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