The US Food and Drug Administration’s (FDA) recent approval of TG Therapeutics’ (Nasdaq: TGTX) Briumvi (ublituximab) against relapsing forms of multiple sclerosis (MS) is welcome news for the company after suffering a major setback in 2022 when the FDA extended its review of Briumvi by three months.
However, Briumvi is unlikely to appeal to patients who are already receiving Roche (ROG: SIX) subsidiary Genentech’s Ocrevus ocrelizumab) or Novartis’ (NOVN: VX) Kesimpta (ofatumumab), says GlobalData, a data and analytics company GlobalData.
Briumvi is the third approved injectable MS treatment directed against CD20 antigen expressed on B cells, with the other therapies being Kesimpta (approved in 2020) and Ocrevus (approved in 2017). All three treatments are monoclonal antibodies.
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