LivingGLP1
Study S003310

A Single Dose Pharmacokinetic Study of ray1225 in Subjects With Varying Degrees of Hepatic Impairment

Registration

Registration
NCT06577415
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
UNKNOWN
Enrollment
24
Start
2024-08-26
Primary completion
2025-10-31
Lead sponsor
Guangdong Raynovent Biotech Co., Ltd
Conditions
Hepatic Impairment
Interventions
DRUG:RAY1225
Results posted
FALSE

Registered primary outcomes

  • Pharmacokinetics (PK): Area Under The Drug Concentration-Time Curve From Zero To Infinity (AUC[0-∞]) of RAY1225 [DAY1~43]
  • PK: Maximum Observed Drug Concentration (Cmax) of RAY1225 [DAY1~43]

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