Briumvi (ublituximab-xiiy): A Targeted Therapy for Relapsing Multiple Sclerosis
Immune Modulator | Immunological Agent
Briumvi is a CD20-directed monoclonal antibody used to treat relapsing forms of multiple sclerosis, including clinically isolated syndrome, relapsing-remitting MS, and active secondary progressive disease. By targeting CD20-positive B cells, it helps reduce inflammation and disease activity. Careful pre-treatment screening, infusion protocols, and ongoing monitoring are essential to optimize safety and efficacy.
Mechanism of Action
Briumvi works by targeting CD20-positive B cells, which are believed to play a crucial role in the pathogenesis of multiple sclerosis by contributing to the immune and inflammatory responses.
Administration Protocol
Briumvi is administered as an intravenous infusion. The initial dose is split into two infusions, two weeks apart. Subsequent doses are given every six months. Monitor patients during and after infusions for reactions.
Infusion Reactions
Patients may experience infusion-related reactions. Pre-medicate with corticosteroids, antihistamines, and antipyretics to minimize these risks. Observe patients closely during the first infusion and for at least one hour after.
Screening Before Initiation
Prior to starting treatment with Briumvi, screen patients for hepatitis B virus (HBV) infection as reactivation may occur in carriers of this virus during or after treatment. Also, assess baseline immunoglobulin levels.
Risk of Infections
Given its immunomodulatory effects, Briumvi increases the risk of infections. Teach patients to report symptoms of infection promptly. Avoid live or live-attenuated vaccines during treatment and until B-cell repletion.
PML Warning
Progressive multifocal leukoencephalopathy (PML) has been reported with other CD20-targeting antibodies though not specifically with Briumvi. Monitor patients for neurological symptoms suggestive of PML.
Laboratory Monitoring
Periodic monitoring of blood counts and immunoglobulin levels is recommended, as treatments targeting B cells can cause prolonged hypogammaglobulinemia and an increased risk of infection.
Use in Specific Populations
Exercise caution and monitor pregnant women and nursing mothers closely if treatment with Briumvi is considered necessary.
Patient Education
Inform patients about the potential side effects, signs of infusion reactions, and symptoms of infections. Emphasize the importance of keeping follow-up appointments for regular monitoring.
https://www.tgtherapeutics.com/label-prescribing-info/uspi-briumvi.pdf - prescribing information