10119473 -VIROMARKERS HDV Biomarkers Study

ConditionHDV Infection
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Rome Tor Vergata

About this trial

This is an observational study, in which clinical data, samples, and any other procedures possibly already performed on participants, were performed within the scope of clinical practice or within the scope of otherwise authorized projects, and that therefore there are no procedures performed specifically for this study, which instead uses data collected previously or prospectively during an extended follow-up, but in any case within the scope of current clinical practice. Most participants have been enrolled and followed up at the project partners' clinical sites over 2023-2025. Their follow-up and sample collection will continue over the duration of the project. At the time of enrollment, demographics, medical history, medications and treatments prescribed were recorded and will be used in this study if the participant consent to be included also in VIROMARKERS. HDV genotypes/subgenotypes will be determined ex-novo on existing baseline stored samples.

The harmonization of HDV-RNA assays by utilizing standardized and validated flowcharts still represents a relevant diagnostic unmet clinical need for the appropriate monitoring of patients with CHD receiving BLV treatment. Furthermore, information on long-term virological response and factors predictive of virological outcome is scarce.

Specific primary objectives to characterise the response to bulevirtide in CHD include:

* To estimate the percentage of participants who will achieve virological response (defined as a decline in serum HDV RNA of \>2 log or to undetectable HDV-RNA) and the proportion achieving undetectable HDV-RNA at week 48, 96 and 144 weeks of BLV treatment. * To estimate the percentage of participants who will achieve biochemical response and combined response (defined as achievement of virological response and ALT normalization) at week 48, 96 and 144 weeks of BLV treatment. * To evaluate whether HDV-RNA levels at baseline or their kinetics during the first 12 weeks of BLV treatment can predict the achievement of undetectable serum HDV-RNA during BLV treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Be > 18 years of age

Sign an informed consent

Have a diagnosis of HDV infection with or without compensated cirrhosis

Having started BLV monotherapy 2mg/day according to the criteria reported in the recent clinical practice guidelines on HDV infection promoted by EASL (EASL CPG 2023)

Disqualifiers

Decompensated liver disease

BLV combined with pegIFN

Past treatment with BLV

Trial population

participants have to be ≥18 years of age, have signed an informed consent and satisfy the following additional criteria: A diagnosis of chronic HDV infection with or without compensated cirrhosis Having started BLV monotherapy 2mg/day according to the criteria reported in the recent clinical practice guidelines on HDV infection promoted by EASL \[EASL CPG 2024\] Be under effective treatment with nucleoside analogues with HBV-DNA \<20 IU/ml at the time of starting BLV

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

220 Participants
are grouped into 1 trial group
Group A: HDV-BLV

Trial outcomes

Primary outcomes

1

HDV Viral Load

HDV-RNA decline \> 2 log OR reaching undetectable HDV-RNA

Time frame
48, 96, 144 weeks after starting Bulevirtide

Secondary outcomes

Other outcomes

Sponsors and contacts

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University of Rome Tor Vergata

Lead sponsor

Euresist Network GEIE

Collaborator

Informapro Srl

Collaborator

Royal Free and University College Medical School

Collaborator

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Collaborator

EUROPEAN LIVER PATIENTS ASSOCIATION

Collaborator

This trial is not recruiting at the moment. You can still explore other options: