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A Study to Evaluate Tobevibart + Elebsiran in Chronic HDV Infection

← catalyst calendar

NCT06903338 · readout in 134 d

Sponsored by Vir Biotechnology, Inc. (industry) · VIR — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
124actual
Sites
39
Countries
Canada, Georgia, Germany +7

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-03-12actualWhen the study began enrolling
Primary completion2026-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMay 2031estimatedThe whole study's end, after follow-up
First posted2025-03-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Viral Hepatitis

Interventions

  • Drug: Tobevibart — also filed as VIR-3434
  • Drug: Elebsiran — also filed as VIR-2218

Primary outcomes

what the primary-completion date above is the date OF
HDV RNA < Lower Limit of Quantification (LLOQ), Target Not Detected (TND) and alanine aminotransferase (ALT) normalization (ALT </= Upper Limit of Normal [ULN]) at Week 48 for Arm 1 vs at Week 12 for Arm 2
measured Up to 48 weeks
Incidence of Treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) through Week 12
measured Up to 12 weeks

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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