Chronic Hepatitis D Infection

3

Review clinical trials related to Chronic Hepatitis D Infection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Trial Evaluating Brelovitug (BJT-778) vs Bulevirtide for the Treatment of Chronic Hepatitis Delta Infection (AZURE-2)

This is a Phase 3, global, randomized, open-label, multicenter, trial evaluating brelovitug (BJT-778) vs bulevirtide for the treatment of chronic hepatitis delta infection (CHD). The main goal of this study is to test the effectiveness of brelovitug compared to bulevirtide as a long-term treatment in patients with chronic HDV infection.

Participants needed: 172
Trial details
Phase: Phase 3Age: 18-99Biological sex: AllType: InterventionalSponsor: Mirum Pharmaceuticals, Inc.Updated: Jun 15, 2026Locations: 48
Eligibility criteria

Willing and able to provide written informed consent [+4]

Pregnant or nursing females [+5]

Status: Recruiting

A Phase III Study to Evaluate the Efficacy and Safety of Libevitug in Participants With Chronic HDV Infection (D-clear Study)

This is an international, multicenter, randomized, controlled, open-label Phase III trial. It will evaluate the efficacy and safety of libevitug in participants with chronic HDV infection.

Participants needed: 160
Trial details
Phase: Phase 3Age: 12-70Biological sex: AllType: InterventionalSponsor: Huahui HealthUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Willing to sign written informed consent; [+4]

Concomitant decompensated cirrhosis; [+6]

Status: Recruiting

Find HDV and Determine Its Status in Turkey

The aim of these study to determine the prevalence of hepatitis Delta virus (HDV) infections and the prognosis of HDV patients in Turkey's southeast. The investigators intend to arrange training sessions for 250 family physicians in Diyarbakir, Batman, Mardin, and Sanliurfa in order to determine those goals. The investigators will talk about diagnosing hepatitis B virus (HBV), HDV, hepatitis C virus (HCV), and Human Immunodeficiency virus (HIV) infections during these events. To ensure that patients with simultaneous HDV infection are evaluated for HIV/HCV and to detect liver fibrosis with a non-invasive method.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Yaşar Bayındır, MDUpdated: Aug 12, 2024Locations: 2Duration: 13 Months
Eligibility criteria

Adults (Age≥18) [+2]

There are no exclusion criteria in this study.