Pharmacokinetics of Leritrelvir(Ray1216) in Elder Participants
NCT06169085 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 32
Last updated 2024-04-16
Summary
The purpose of this study is to assess the safety, tolerability and PK of Leritrelvir in elder participants
Conditions
- Elder
Interventions
- DRUG
-
Leritrelvir
Oral
Sponsors & Collaborators
-
Guangdong Raynovent Biotech Co., Ltd
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 15 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-08-24
- Primary Completion
- 2023-09-20
- Completion
- 2023-10-11
Countries
- China
Study Locations
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