LivingGLP1
Study S003267

An Open-Label, Parallel-Group, Single-Dose Pharmacokinetic Study of HRS-4729 Injection in Healthy Participants and Patients With Renal Impairment

Registration

Registration
NCT07807059
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
RECRUITING
Enrollment
32
Start
2026-09-09
Primary completion
2027-03-15
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Overweight/Obesity; Metabolic Dysfunction-associated Steatotic Liver Disease/Steatohepatitis (MASLD/MASH); Type 2 Diabetes Mellitus
Interventions
DRUG:HRS-4729
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Cmax [assessed up to approximately 4 weeks post-dose;]
  • AUC0-t [assessed up to approximately 4 weeks post-dose]
  • AUC0-inf. [assessed up to approximately 4 weeks post-dose]

Linked records (0)

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