LivingGLP1
Study S000893

Investigation of Pharmacokinetics and Safety of HRS-7535 in Subjects With Mild and Moderate Hepatic Impairment and Normal Hepatic Function

Registration

Registration
NCT06961643
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
24
Start
2025-06-05
Primary completion
2026-01-22
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Diabetes Mellitus
Interventions
DRUG:HRS-7535 Tables
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • The maximum plasma concentration of HRS-7535 (Cmax) [Post-dose at day 1 to day 4.]
  • Area under the concentration curve from time 0 to the last quantifiable concentration (AUC0-t) [Post-dose at day 1 to day 4.]
  • Area under the concentration curve from time 0 to extrapolated infinite time (AUC0-inf) [Post-dose at day 1 to day 4.]

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