A Trial of HRS-1893 in Healthy Volunteers
NCT07033455 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2025-11-18
Summary
The purpose of this study is to assess the safety and PK characteristics of a single oral dose of HRS-1893 in healthy voluunters.
Conditions
Interventions
- DRUG
-
HRS-1893
Single dose of HRS-1893 orally administered
Sponsors & Collaborators
-
Atridia Pty Ltd.
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-06-25
- Primary Completion
- 2025-09-05
- Completion
- 2025-10-30
Countries
- Australia
Study Locations
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