Fenofibrate in Primary Biliary Cholangitis: a Real World Study
NCT06755151 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2026-01-08
Summary
An Open Label Long-Term Study to Evaluate the Safety and Tolerability of Fenofibrate in Combination with Ursodeoxycholic Acid in Subjects with Primary Biliary Cholangitis (PBC)
Conditions
- Primary Biliary Cholangitis (PBC)
Interventions
- DRUG
-
Fenofibrate
Fenofibrate 200mg
Sponsors & Collaborators
-
Xijing Hospital of Digestive Diseases
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-17
- Primary Completion
- 2035-12-31
- Completion
- 2035-12-31
Countries
- China
Study Locations
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