LivingGLP1
Study S001592

A Multi-center, Single-dose, Parallel-group, Open-label Study to Evaluate the Pharmacokinetics of HRS9531 Injection in Participants With Mild, Moderate, and Normal Hepatic Function

Registration

Registration
NCT07540754
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
RECRUITING
Enrollment
24
Start
2026-05-26
Primary completion
2027-01
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Diabetes Mellitus; Weight Loss
Interventions
DRUG:HRS9531 Injection
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Maximum concentration (Cmax) [Post-dose from Day 1 to Day 29.]
  • The area under the concentration-time curve to the last measurable concentration (AUClast) [Post-dose from Day 1 to Day 29.]
  • The area under the concentration-time curve extrapolated to infinity (AUCinf) [Post-dose from Day 1 to Day 29.]

Linked records (0)

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