Expanded Access for Bulevirtide

NCT06780579 · Status: AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2026-03-20

No results posted yet for this study

Summary

The goal of this study is to provide access to bulevirtide (BLV (GS-4438), Hepcludex®) to eligible participants with chronic hepatitis delta virus infection (CHD).

Conditions

  • Chronic Hepatitis Delta Virus Infection

Interventions

DRUG

Bulevirtide

10 mg BLV will be administered via subcutaneous injection

Sponsors & Collaborators

Principal Investigators

  • Gilead Study Director · Gilead Sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06780579 on ClinicalTrials.gov