Incidence of Viral Hepatitis D Relapses Upon Discontinuation of Bulevirtide in Patients With Chronic Hepatitis D and Negative HDV RNA

Chronic Hepatitis D Clinical Trial

Official title:

A Prospective, Observational Clinical Study to Evaluate the Incidence of Viral Hepatitis D Relapses Upon Discontinuation of Antiviral Therapy With Bulevirtide in Patients With Chronic Hepatitis D and Negative HDV RNA

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06121427
• Other study ID #: CTT-001
• Status: Recruiting
• Start date: September 1, 2023
• Est. completion date: February 28, 2025

Study information

• Verified date: November 2023
• Source: Center of target therapy
• Contact: Pavel Bogomolov, MD
• Phone: +7 495 320 06 66
• Email: bogomolov.po[@]ums-03.ru
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This observational study will be conducted in patients with chronic co-infection with hepatitis B and D viruses, with negative PCR for HDV RNA in peripheral blood and no signs of active liver inflammation according to blood chemistry parameters, receiving background therapy with bulevirtide for more than 48 weeks and liver biopsy performed or prescribed to be performed as part of routine practice. After the patient has signed the Informed Consent, a portion of the liver biopsy collected as part of routine practice will be sent to the laboratory for PCR testing for HDV RNA, background therapy with bulevirtide will be interrupted, and the patient will be observed in the clinic in accordance with routine medical practice, but at least once times every 4 weeks, for timely detection of relapse of the hepatitis D and initiation of antiviral therapy. Once a relapse of viral hepatitis D is determined via the PCR HDV RNA, the patient's participation in the study will be terminated. The collected data will be analyzed to assess the probability of relapse-free over time. Separate tests will also be conducted for subgroups of patients based on covariates such as duration of previous background therapy with bulevirtide, duration of HDV suppression, use of any other concomitant antiviral therapy during bulevirtide treatment.

Description:

The main goal of this study is the following: - To assess the probability of HDV relapse-free over time after discontinuation of background therapy with bulevirtide in patients with chronic co-infection with hepatitis B and D viruses and negative PCR HDV RNA Primary endpoint: Occurrence of hepatitis D viral relapse. Additional objectives in this study: - Analyze data on the time of relapse and the duration of previous background therapy with bulevirtide, the duration of the period of HDV suppression, and the use of any other concomitant antiviral therapy during the period of treatment with bulevirtide - Analyze relapse-free patients over 96 weeks of study follow-up - Analyze the results of qualitative PCR (positive / negative) for hepatitis D virus RNA in a liver biopsy before discontinuing bulevirtide therapy

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: February 28, 2025
• Est. primary completion date: February 28, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Informed consent of the patient to participate in the study, collect and use data
• Age 18 or older
• Background therapy with bulevirtide for at least 48 weeks
• Negative qualitative PCR test for RNA of viral hepatitis D in peripheral blood before inclusion in the study
• No active liver inflammation
• Liver biopsy performed as part of routine practice (no older than 3 weeks before inclusion in the study) or prescribed biopsy to be performed before bulevirtide interruption

Exclusion Criteria:

• Liver damage not related to viral hepatitis B and D - autoimmune hepatitis, drug or alcohol liver damage, Wilson-Konovalov disease, etc.
• Co-infection with hepatitis C virus
• Patients receiving HBV and HDV therapy not in accordance with standard practice or violations of the Instructions for the medical use of the drug/s
• Moderate/severe renal/liver dysfunction
• Lack of informed consent

Related Conditions & MeSH terms

• Chronic Hepatitis D
• Hepatitis
• Hepatitis A
• Hepatitis D
• Hepatitis D, Chronic
• Hepatitis, Chronic

Locations

Country	Name	City	State
Russian Federation	Center of Target Therapy	Moscow

Sponsors (1)

Lead Sponsor	Collaborator
Center of target therapy

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Probability of HDV relapse-free over time	To assess the probability of HDV relapse-free over time discontinuation of background therapy with bulevirtide in patients with chronic co-infection with hepatitis B and D viruses and negative PCR HDV RNA	96 weeks
Secondary	Probability of HDV relapse-free over time and the duration of previous background therapy with boulevertide	Analyze the probability of HDV relapse-free over time and the duration of previous background therapy with boulevertide	96 weeks
Secondary	Probability of HDV relapse-free over time and the duration of the period of HDV suppression	Analyze the probability of HDV relapse-free over time and the duration of the period of HDV suppression	96 weeks
Secondary	Probability of HDV relapse-free over time and the use of any other concomitant antiviral therapy during the period of treatment with bulevirtide	Analyze the probability of HDV relapse-free over time and the use of any other concomitant antiviral therapy during the period of treatment with bulevirtide	96 weeks
Secondary	Relapse-free patients over 96 weeks	Analyze HDV relapse-free patients over 96 weeks	96 weeks
Secondary	Results of qualitative PCR HDV RNA in a liver biopsy	Analyze the results of qualitative PCR HDV RNA (positive / negative) in a liver biopsy before discontinuing bulevirtide therapy	Baseline (At the time of the patient inclusion)