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Study identifier: NCT07364448 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Evaluate the Safety of Hydronidone Capsules in Patients With Liver Fibrosis

Condition: Chronic Hepatitis B With Hepatic Fibrosis  ·  Sponsor: Beijing Continent Pharmaceutical Co, Ltd.

PhasePhase 2
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is an open-label, single-arm study designed to collect safety data on hydronidone capsules in patients with chronic hepatitis B virus infection accompanied by liver fibrosis or fatty liver disease accompanied by liver fibrosis . Approximately 200 subjects will be enrolled, all of whom will receive hydronidone capsules three times daily, with three capsules per dose, resulting in a total daily treatment dose of 270 mg. The medication will be administered orally half an hour before meals for a total of 28 days.

This description comes directly from the study's public registry record.

Talk to the study team

Ling Zhang  ·  +86-13501209210  ·  zhangling@bjcontinent.com

Always discuss trial participation with your own doctor first.

Locations (1)

Jilin University First HospitalJilin City, Changchun, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07364448