LivingGLP1
Study S000968

Pharmacokinetics of IBI362 in Subjects With and Without Renal Impairment

Registration

Registration
NCT05793450
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
20
Start
2023-05-05
Primary completion
2023-09-18
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Renal Impairment
Interventions
DRUG:IBI362
Results posted
FALSE

Registered primary outcomes

  • Pharmacokinetics (PK): Maximum Concentration (Cmax) of IBI362 [Predose through 1344 hours postdose]
  • PK: Area Under the Concentration Versus Time Curve (AUC) of IBI362 [Predose through 1344 hours postdose]

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.