MS Breakthrough: Thousands of Patients in England Gain Access to New 'Wonder Drug'

Published 3 days ago3 minute read
Precious Eseaye
Precious Eseaye
MS Breakthrough: Thousands of Patients in England Gain Access to New 'Wonder Drug'

Thousands of individuals in England living with a specific type of multiple sclerosis (MS) are poised to receive significant benefits from a newly approved treatment on the NHS. Natalizumab, administered either as an infusion or injection every four weeks, has been officially recommended by the National Institute for Health and Care Excellence (NICE). This treatment will be available as a crucial option for patients diagnosed with relapsing-remitting MS (RRMS), which represents the most prevalent form of the condition characterized by intermittent symptom flare-ups.

A particularly noteworthy aspect of this recommendation is its safety profile for women planning to start a family, as Natalizumab can be taken during pregnancy. This offers a vital advantage over other highly effective disease-modifying therapies (DMTs) which may not be suitable for use during gestation. Patients will have access to Natalizumab in situations where their MS remains highly active despite prior therapies, or when other existing treatments are deemed unsuitable for their individual circumstances.

Multiple sclerosis is fundamentally an autoimmune disease where the body's immune cells mistakenly attack myelin, the protective insulating layer surrounding nerves in the brain and spinal cord. This erroneous attack triggers inflammation and subsequent scarring, leading to a diverse range of symptoms including vision impairment, muscle weakness, profound fatigue, and issues with balance and coordination. Natalizumab exerts its therapeutic effect by binding to immune cells, thereby keeping them confined within the bloodstream and preventing their detrimental entry into the brain and spinal cord, where they would otherwise cause damage.

According to NICE estimates, approximately 123,000 people in England are living with MS, with an estimated 43,000 experiencing RRMS at any given time. The condition is notably more common in women, with a prevalence approximately three times higher than in men. Two distinct versions of Natalizumab have received approval for NHS use: Tysabri, manufactured by Biogen, which is administered as an injection, and Tyruko, produced by Sandoz, delivered via infusion.

Helen Knight, Director of Medicines Evaluation at NICE, expressed the significance of this development, stating that it provides people living with highly active relapsing-remitting MS with a meaningful additional treatment option. She underscored the importance of having choice for individuals managing a lifelong condition, enabling them and their clinicians to select the most appropriate treatment based on personal circumstances. Ceri Smith, Head of Policy at the MS Society, echoed these sentiments, highlighting the particular benefit for women with MS who wish to become pregnant, due to Natalizumab's pregnancy-safe profile.

Professor Ruth Dobson, Centre Lead for the Centre of Preventive Neurology at the Wolfson Institute of Population Health, welcomed the news, acknowledging that it offers a wider array of treatments to thousands experiencing breakthrough MS activity, without unnecessary delays. This expanded choice empowers patients and their healthcare providers to collaboratively choose the most suitable treatment. James Palmer, Medical Director for Specialised Services at NHS England, emphasized that for those grappling with highly active multiple sclerosis, finding an effective treatment can profoundly improve their daily lives. He concluded that this NICE recommendation equips patients and their specialist teams with another potent option when the disease persists despite other treatments, fostering more personalized care and informed decision-making.

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