NICE recommends Briumvi for RRMS

5 December 2024

Germany-headquartered CNS drug specialist Neuraxpharm today revealed that UK health technology assessor the National Institute for Health and Care Excellence (NICE) has issued a positive recommendation for the use of ublituximab (150mg concentrate for solution for infusion) in the treatment of relapsing-remitting multiple sclerosis (RRMS).

.Ublituximab, trade named Briumvi, developed by TG Therapeutics (Nasdaq: TGTX) and licensed by Neuraxpharm ex-US, is a type of protein called a monoclonal antibody that selectively targets CD-20-expressing cells. It is the first and only anti-CD20 monoclonal antibody approved in the USA and European Union (EU) for adult patients with RRMS that can be administered in a one-hour infusion, twice a year, following the starting dose.2,5,6

Clinical backing

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