Clinical Trial

Drug-Drug Interaction Study Between Hydronidone and Entecavir, Tenofovir Disoproxil Fumarate, Tenofovir Alafenamide, and Tenofovir Amibufenamide

Completed Phase 1
View on ClinicalTrials.gov →
Summary
The proposed indication for Hydronidone Capsules is chronic hepatitis B-associated liver fibrosis, which in clinical practice typically requires concomitant use with antiviral agents for chronic hepatitis B. The commonly used chronic hepatitis B antiviral agents include Entecavir, Tenofovir Disoproxil Fumarate (TDF), Tenofovir Alafenamide (TAF), and Tenofovir Amibufenamide (TMF). This study aims to evaluate the drug-drug interaction (DDI) of Hydronidone Capsules 90 mg with Entecavir, Tenofovir Disoproxil Fumarate (TDF), Tenofovir Alafenamide (TAF), and Tenofovir Amibufenamide (TMF) respectively in healthy participants, to inform the preparation of post-marketing labeling and the development of concomitant dosing regimens in clinical practice.
Protocol Amendment History 3 changes
critical Completed without a posted recruiting period 2026-08-14
notable Primary completion moved earlier: 2026-06-30 -> 2026-05-29 2026-08-14
minor Completion moved earlier: 2026-06-30 -> 2026-05-29 2026-08-14
Trial Details
NCT Number NCT07295873
Lead Sponsor Beijing Continent Pharmaceutical Co, Ltd.
Conditions Chronic Hepatitis B Liver Fibrosis, DDI (Drug-Drug Interaction)
Enrollment 64 participants
Start Date 2026-03-15
Primary Completion 2026-05-29 (estimated)
Study Completion 2026-05-29 (estimated)
Updated on ClinicalTrials.gov 2026-08-13