CS0159 in Chinese Patients With PBC (Primary Biliary Cholangitis)
NCT05896124 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 75
Last updated 2026-03-13
Summary
A phase II study to evaluate safety, tolerability and efficacy of CS0159 in patients with PBC (Primary Biliary Cholangitis).
Conditions
- Primary Biliary Cholangitis (PBC)
Interventions
- DRUG
-
2mg CS0159
Oral QD
- DRUG
-
Oral QD
Sponsors & Collaborators
-
Cascade Pharmaceuticals, Inc
lead OTHER
Principal Investigators
-
Rong Deng · Cascade Pharmaceuticals, Inc
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-08-07
- Primary Completion
- 2025-12-31
- Completion
- 2026-03-15
Countries
- China
Study Locations
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