Vir Biotechnology Receives FDA IND Clearance and Fast Track Designation for Tobevibart and Elebsiran for the Treatment of Chronic Hepatitis Delta Infection
Vir's hepatitis D therapy has shown efficacy in a phase 2 test, suggesting the cocktail may pose a threat to Gilead’s attempt in the market.
Tobevibart Monotherapy and Combination Therapy with Elebsiran Achieved High Virologic Response and ALT Normalization in People Living with the Hepatitis Delta Virus After 12 and 24 Weeks of Treatment
Vir Biotechnology to Participate in the Goldman Sachs 45th Annual Global Healthcare Conference
Vir Biotechnology Appoints Mark Eisner, M.D., M.P.H. as Chief Medical Officer
Vir Biotechnology to Host 2024 Annual Meeting of Stockholders
Multiple Abstracts Highlighting Vir Biotechnology’s Latest Hepatitis Delta & B Data Accepted for Presentation at the EASL Congress 2024
Vir Biotechnology Announces SOLSTICE Data to be Featured as an Oral Presentation at the European Association for the Study of the Liver (EASL) Congress 2024
Vir Biotechnology Provides Corporate Update and Reports First Quarter 2024 Financial Results
Vir Biotechnology to Participate in the BofA Securities Healthcare Conference 2024