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A Phase 2 Trial of Foscenvivint in Liver Cirrhosis Patients Caused by HIV/HCV Co-infection With Hemophilia (OP-724-H201)

Liver Cirrhosis Clinical Trial

Official title:
A Multi-center, Single-arm, Open-label Phase 2 Trial of Foscenvivint in Liver Cirrhosis Patients Caused by HIV/HCV Co-infection With Hemophilia

Clinical Trial Summary

This is a phase 2 trial of foscenvivint in liver cirrhosis patients caused by HIV/HCV co-infection with hemophilia to evaluate the efficacy, safety and pharmacokinetics.

Clinical Trial Description

This is designed a multi-center, single-arm, open-label trial of foscenvivint administered intravenously twice a week for 24 weeks. A follow up visit will be conducted 4 weeks after the last administration. Liver cirrhosis patients due to co-infection of HIV and HCV with hemophilia who have a Child-Pugh classification of A or B are included. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06144086
Study type Interventional
Source Komagome Hospital
Contact Kiminori Kimura, MD
Phone +81-3-3823-2101
Email kiminori_kimura@tmhp.jp
Status Recruiting
Phase Phase 2
Start date May 8, 2024
Completion date June 30, 2025
View Details
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