Vir Biotechnology, Inc. announced that the US Food and Drug Administration (FDA) has cleared its investigational new drug application and granted Fast Track designation for the combination of tobevibart and elebsiran for the treatment of chronic hepatitis delta infection. Tobevibart, an investigational monoclonal antibody, and elebsiran, an investigational small interfering ribonucleic acid, are currently being evaluated in the Company’s Phase 2 SOLSTICE hepatitis delta clinical trial, with complete 24-week treatment data on track to be reported in the fourth quarter.
Read the full press release here.
Source : Vir Biotechnology, Inc.
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