A Study of the Pharmacokinetics and Safety of CS0159 in Subjects With Hepatic Injury
NCT06888115 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2025-07-11
Summary
Phase I Study of the Pharmacokinetics and Safety of CS0159 in Subjects With Hepatic Injury
Conditions
Interventions
- DRUG
-
CS0159
Single oral dose of CS0159 4mg
Sponsors & Collaborators
-
Cascade Pharmaceuticals, Inc
lead OTHER
Principal Investigators
-
Zhao wei feng, Master · The First Affiliated Hospital of Soochow University
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-03-13
- Primary Completion
- 2025-05-29
- Completion
- 2025-06-03
- FDA Drug
- Yes
Countries
- China
Study Locations
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