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Clinical Trial Summary

1. Evaluate the pharmacokinetic (PK) characteristics of Hydronidone capsule in target patients (patients with chronic viral hepatitis b with liver fibrosis) and special population (patients with mild liver dysfunction). 2. To evaluate the effect of oral Hydronidone capsule on QT/QTc in patients with chronic viral hepatitis b accompanied by hepatic fibrosis and mild hepatic dysfunction.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04123769
Study type Interventional
Source Beijing Continent Pharmaceutical Co, Ltd.
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Status Completed
Phase Phase 1
Start date September 3, 2019
Completion date January 30, 2021