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RECRUITING
NCT05749822
PHASE2/PHASE3

Fenofibrate for Compensated Cirrhosis Patients With Primary Biliary Cholangitis

Sponsor: Xijing Hospital of Digestive Diseases

View on ClinicalTrials.gov

Summary

The main objectives of the study were to assess the effects of fenofibrate on serum alkaline phosphatase, as a composite endpoint and on safety in participants with primary biliary cholangitis (PBC).

Official title: Fenofibrate Combined With Ursodeoxycholic Acid in Compensated Cirrhosis Patients With Primary Biliary Cholangitis Who Had an Inadequate Response to Ursodeoxycholic Acid

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

104

Start Date

2023-02-17

Completion Date

2027-12-31

Last Updated

2026-01-08

Healthy Volunteers

No

Interventions

DRUG

Fenofibrate 200mg

Fenofibrate 200mg/day

DRUG

Placebo

1 tablet/ day

DRUG

UDCA

UDCA 13-15mg/kg/day

Locations (12)

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China

Sun Yat-sen Memorial Hospital

Guangzhou, Guangdong, China

Henan Provincial People's Hospital

Zhengzhou, Henan, China

Xiangya Hospital Central South University

Changsha, Hunan, China

Jiangsu Province Hospital

Nanjing, Jiangsu, China

The First Hospital of China Medical University

Shenyang, Liaoning, China

Xijing Hospital

Xi'an, Shaanxi, China

Yan'an University Affiliated Hospital

Yan’an, Shaanxi, China

Sichuan Provincial People's Hospital

Chengdu, Sichuan, China

Tianjin Third Central Hospital

Tianjin, Tianjin Municipality, China

The Second Affiliated Hospital of Kunming Medical University

Kunming, Yunnan, China

Tianjin Medical University General Hospital

Tianjin, China