Drug intelligence / Profile preview

tobevibart + elebsiran

Development stage
Unknown
Lead developer
Vir Biotechnology
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Subcutaneous
01

Overview

Tobevibart + elebsiran is an investigational combination therapy for chronic hepatitis delta (CHD) and chronic hepatitis B. Tobevibart is a broadly neutralizing monoclonal antibody targeting the hepatitis B surface antigen; it inhibits the entry of both hepatitis B virus (HBV) and hepatitis delta virus (HDV) into hepatocytes and reduces circulating viral particles. Elebsiran (also known as VIR-2218) is a small interfering RNA (siRNA) designed to degrade HBV RNA transcripts, thereby limiting production of the hepatitis B surface antigen and exerting direct antiviral activity against both HBV and HDV. Both agents are administered subcutaneously. The combination has demonstrated rapid, deep suppression of HDV RNA in clinical trials, with 100% of participants in the combination arm achieving significant virologic response at week 24 in phase 2 studies. The therapy has received FDA Breakthrough Therapy designation and EMA PRIME designation for CHD[1][3][5][6].

Other names
tobevibart-elebsiran
02

Targets

HBsAg (Hepatitis B surface antigen)

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