EMA Recommends Novartis' Meningitis B Vaccine for Approval
The European Medicines Agency's Committee for Medicinal Products for Human Use has recommended Novartis' meningitis B vaccine, Bexsero, for approval for patients aged 2 months or older. This vaccine represents a significant advancement in preventing meningococcus B bacterium, the leading cause of meningitis in industrialized countries. If approved, Bexsero could drastically reduce the incidence of childhood meningitis and septicemia.
The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recently recommended Novartis’ meningitis B vaccine, Bexsero, for approval. This recommendation is for the vaccine's use in patients aged 2 months or older, marking a pivotal moment in the fight against meningococcus B bacterium, the primary cause of meningitis in industrialized nations.
Bacterial meningitis is a severe infection that leads to approximately 170,000 deaths worldwide each year, according to the World Health Organization (WHO). The recommendation for Bexsero's approval by the CHMP is a significant milestone, as it could become the first vaccine to protect against the meningococcus B bacterium.
Dr. Matthew Snape, Consultant in Pediatrics and Vaccinology at the Oxford Vaccine Group, University of Oxford, emphasized the importance of this development: "MenB disease is a major cause of meningitis and septicemia in children, and its ability to cause a rapidly progressive, devastating illness makes it one of the infections most feared by both parents and pediatricians. A vaccine that is able to reduce the incidence of this disease would be a major advance towards the prevention of childhood meningitis."
Andrin Oswald, Division Head of Novartis Vaccines and Diagnostics, highlighted the company's dedication to combating MenB disease: "We are proud of the major advance that Bexsero represents within the field of vaccine development against what up until now has been a very challenging disease target. For over two decades, our researchers and clinicians have been dedicated to finding a solution to prevent MenB disease. Our steadfast determination has been inspired by the testimonies from survivors and families who have lost loved ones to this disease."
The European Commission typically follows the CHMP's recommendations within three months. If approved, Bexsero will not only mark a significant achievement for Novartis but also offer hope to countless families affected by meningitis B. This recommendation comes at a crucial time for Novartis, as it seeks to reinforce its position in the vaccines and pharmaceuticals space following recent challenges.
Novartis remains optimistic about its future, with a recent statement projecting the production of 14 or more blockbuster drugs in the next five years. The potential approval of Bexsero represents a key step in this direction, underscoring the company's commitment to addressing unmet medical needs through innovative vaccine development.

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EMA recommends Novartis' meningitis B vaccine for approval
pharmaphorum.com · May 16, 2025
The European Medicines Agency’s Committee for Medicinal Products for Human Use recommends Novartis’ meningitis B vaccine...