Pharmacokinetics of Leritrelvir(RAY1216) in Participants With Hepatic Impairment
NCT06161259 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2023-12-07
Summary
This study will assess the effect of hepatic impairment on the pharmacokinetics (PK), safety and tolerability of Leritrelvir(RAY1216)
Conditions
- Hepatic Impairment
Interventions
- DRUG
-
Leritrelvir(Ray1216)
Participants receive Leritrelvir orally.
Sponsors & Collaborators
-
Guangdong Raynovent Biotech Co., Ltd
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-09-14
- Primary Completion
- 2023-10-01
- Completion
- 2023-10-07
Countries
- China
Study Locations
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