A Trial of HRS-9813 in Healthy Volunteers
NCT06514963 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2025-01-08
Summary
The purpose of this phase Ⅰ study is to evaluate the safety, tolerability and pharmacokinetics of HRS-9813 in healthy volunteers.
Conditions
- Healthy Volunteers
Interventions
- DRUG
-
HRS-9813
Specified dose on specified days
- DRUG
-
Specified dose on specified days
Sponsors & Collaborators
-
Guangdong Hengrui Pharmaceutical Co., Ltd
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-07-24
- Primary Completion
- 2025-01-02
- Completion
- 2025-01-02
Countries
- China
Study Locations
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