drugset / Trial / NCT06903338

A Study to Evaluate Tobevibart + Elebsiran in Chronic HDV Infection

NCT06903338

Phase 3 Active not recruiting 124 enrolled Vir Biotechnology, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, open label, randomized Phase 3 clinical study to evaluate the efficacy and safety of the combination of tobevibart + elebsiran for the treatment of chronic hepatitis delta in comparison to delayed treatment.

Timeline

Start
2025-03-12
Primary completion
2026-12-31
Completion
2031-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tobevibart Monoclonal antibody Subcutaneous
Subject VIR-2218 Small interfering RNA (siRNA) Subcutaneous

Indications