RecruitingPhase 3NCT06755541

Fenofibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cholangitis: a Real World Study

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)


Sponsor

Xijing Hospital of Digestive Diseases

Enrollment

150 participants

Start Date

Jan 30, 2024

Study Type

INTERVENTIONAL

Conditions

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)


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Fenofibrate in Combination With Ursodeoxycholic Acid for people with primary biliary cholangitis (pbc). The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 75 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFenofibrate in Combination With Ursodeoxycholic Acid

Experimental: Fenofibrate 200 mg Capsules


Locations(1)

Xijing hospital

Xi'an, Shaanxi, China

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NCT06755541


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