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RECRUITINGOBSERVATIONAL

New HBV Infection Biomarkers: Clinical Characterization and Impact on Management

New Biomarkers of HBV Infection: Clinico-Biological Characterization and Impact on Infection Management

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Chronic Hepatitis B Virus (HBV) infection affects nearly 300 million people worldwide and is a leading cause of liver fibrosis, cirrhosis, and hepatocellular carcinoma (HCC). In France, it affects around 0.3% of the population. Current clinical practice relies on traditional biomarkers, such as HBV DNA and HBsAg, to monitor viral replication and disease progression. However, these biomarkers do not fully capture the viral activity or predict clinical outcomes. Recently, new biomarkers like HBcrAg and HBV RNA have emerged, showing promise for better understanding the natural history of the infection and guiding treatment decisions. The main objective of this research is to evaluate the predictive role of these biomarkers (HBcrAg, HBV RNA) in HBV-infected patients, focusing on their association with HBsAg seroconversion and their ability to predict clinical events like cirrhosis and HCC. Secondary objectives include describing the clinicobiological characteristics of patients, determining HBV genotypes, characterizing the impact of HBV on the host's transcriptome, and studying the biomarkers' role in different phases of the infection and treatment. The ultimate goal is to identify more accurate biomarkers to guide antiviral treatment, predict disease progression, and potentially determine when treatment can be safely discontinued.

Who May Be Eligible (Plain English)

Who May Qualify: - 18 years old - Chronic HBV infection (HbsAg positive carrier for more than 6 months) - Patient under care within the Henri Mondor-Albert Chenevier University Hospital group Who Should NOT Join This Trial: - History of liver transplantation for liver failure in the context of chronic HBV infection - Protected adults, adults unable to express their consent - Pregnant or breastfeeding women - Person not affiliated with a Social Security system - Patient refusal to participate in the project Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 18 years old * Chronic HBV infection (HbsAg positive carrier for more than 6 months) * Patient under care within the Henri Mondor-Albert Chenevier University Hospital group Exclusion Criteria: * History of liver transplantation for liver failure in the context of chronic HBV infection * Protected adults, adults unable to express their consent * Pregnant or breastfeeding women * Person not affiliated with a Social Security system * Patient refusal to participate in the project

Treatments Being Tested

BIOLOGICAL

Collection of blood samples for the study of HBV biomarkers

The intervention involves the additional and minimal collection of two blood samples during routine care procedures (9mL in a dry tube and 9mL in a Paxgene tube). These samples are specifically collected for research purposes and will be stored in the laboratory at the Henri Mondor Biobank Platform under the responsibility of Pr Bijan Ghaleh-Marzban for 15 years. The samples will be preserved under strict conditions and may be used for future analyses related to the pathology of HBV infection or other scientific advancements, with the patient's informed consent.

Locations (1)

Clinical Research Unit (CRU) Henri Mondor.
Créteil, Créteil, France