The US Food and Drug Administration (FDA) has accepted for review the Biologics License Application (BLA) for ibalizumab as a treatment for multidrug resistant human immunodeficiency virus-1 (MDR HIV-1).
If approved, ibalizumab will be the first antiretroviral treatment (ART) with a new mechanism of action to be introduced in nearly 10 years and the only treatment that does not require daily dosing.Ibalizumab is the first-ever antibody HIV treatment, according to Canadian biotech firm Theratechnologies (TSX: TH), which has licensed right to the drug in the USA and Canada from Taiwan-based TaiMed Biologicals (4147: TT).
Its shares advanced 4.4% to C$8.58 on the news by close of trading Friday, but many investors and traders were already heading off for a long ‘Canada Day’ weekend holiday, so reaction was mute.
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