Clinical Trial

Changes in Bile Acids and Microbiota in Patients With Hepatitis D Treated With Bulvertide

Study acronym: Bio-Delta
Recruiting
View on ClinicalTrials.gov →
Summary
HDV is an RNA virus that infects only in the presence of HBV, affecting about 13% of HBsAg carriers. In Italy, prevalence ranges from 3.2% to 9.3%. It increases the risk of cirrhosis, fulminant hepatitis, and HCC, particularly in high-risk groups (HIV, HCV, drug users, dialysis patients). Until 2020, pegIFN was the only therapy; since 2022, bulevirtide (BLV) has been available, blocking viral entry into hepatocytes and reducing HDV RNA and liver stiffness, with efficacy in 45-48% of patients, though the optimal treatment duration remains uncertain. The gut microbiota and bile acids also play a role in fibrosis and cirrhosis progression: dysbiosis, typical in cirrhotic patients, alters bile acid metabolism and increases intrahepatic toxicity.
Trial Details
NCT Number NCT07429864
Lead Sponsor Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Conditions HBV, HBV Coinfection, HCV, HIV Infections, Hepatocellular Carcinoma, Cirrhosis, Liver, Fibrosis, Liver, Bile Acid Malabsorption +1 more
Enrollment 20 participants
Start Date 2025-09-24
Primary Completion 2027-10 (estimated)
Study Completion 2027-10 (estimated)
Updated on ClinicalTrials.gov 2026-02-24