LivingGLP1
Study S002007

A Multi-center, Single-dose, Open-label, Parallel Design, Pharmacokinetics Study of HRS9531injection in Healthy Subjects and Subjects With Impaired Renal Function

Registration

Registration
NCT06246175
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
32
Start
2024-02-28
Primary completion
2025-09-02
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:HRS9531
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Area Under the Concentration Versus Time Curve (AUC) of HRS9531 From Time Zero to T(last) (AUC0-t) [Start of Treatment up to Day 29]
  • Maximum Concentration of HRS9531 (Cmax) [Start of Treatment up to Day 29]
  • Area Under the Concentration Versus Time Curve (AUC) of HRS9531 From Time Zero to Infinity (AUC0-inf) [Start of Treatment up to Day 29]

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