LivingGLP1
Study S000449

A Single-dose, Open-label/Pharmacokinetic and Safety Studies of HRS-7535 in Subjects With Moderate Renal Insufficiency and Healthy Subjects

Registration

Registration
NCT06132204
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
16
Start
2023-12-21
Primary completion
2024-03-13
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:HRS-7535 Tablets
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • PK parameters of HRS-7535: Cmax [0 hour to 48 hour after administration]
  • PK parameters of HRS-7535: AUC0-t [0 hour to 48 hour after administration]
  • PK parameters of HRS-7535: AUC0-inf [0 hour to Infinity hour after administration]

Linked records (0)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.

No records link to this registration yet.