Condition: Chronic Hepatitis B With Hepatic Fibrosis · Sponsor: Beijing Continent Pharmaceutical Co, Ltd.
This is a single-arm, multicenter, open-label Phase III clinical trial to evaluate the safety and tolerability of high-dose hydronidone capsules in patients with hepatic fibrosis and cirrhosis. Eligible participants will be sequentially enrolled to receive hydronidone capsules 120 mg three times daily (TID) for 28 consecutive days. Participants will return to the hospital on Day 28 after the first dose for a follow-up safety assessment. All adverse events (AEs) and concomitant medications must be recorded during the study period. Participants who complete the Day 28 follow-up visit are considered to have completed the study.
This description comes directly from the study's public registry record.
Ling Zhang · +86-13501209210 · zhangling@bjcontinent.com
Always discuss trial participation with your own doctor first.
| The Sixth People's Hospital of Zhengzhou City | Zhengzhou, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07343778