{"id":2563001,"date":"2023-08-29T11:49:31","date_gmt":"2023-08-29T15:49:31","guid":{"rendered":"https:\/\/platoai.gbaglobal.org\/platowire\/roches-evrysdi-receives-european-commission-approval-for-treating-spinal-muscular-atrophy-in-infants\/"},"modified":"2023-08-29T11:49:31","modified_gmt":"2023-08-29T15:49:31","slug":"roches-evrysdi-receives-european-commission-approval-for-treating-spinal-muscular-atrophy-in-infants","status":"publish","type":"platowire","link":"https:\/\/platoai.gbaglobal.org\/platowire\/roches-evrysdi-receives-european-commission-approval-for-treating-spinal-muscular-atrophy-in-infants\/","title":{"rendered":"Roche\u2019s Evrysdi Receives European Commission Approval for Treating Spinal Muscular Atrophy in Infants"},"content":{"rendered":"

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Roche’s Evrysdi, also known as risdiplam, has recently received approval from the European Commission for the treatment of spinal muscular atrophy (SMA) in infants. This approval marks a significant milestone in the fight against this rare genetic disorder, offering new hope for infants and their families.<\/p>\n

SMA is a debilitating neuromuscular disease that affects approximately one in every 10,000 live births. It is characterized by the loss of motor neurons in the spinal cord, leading to progressive muscle weakness and atrophy. Infants with SMA often experience difficulty with basic motor functions such as sitting, crawling, and walking. In severe cases, the disease can also affect the muscles involved in breathing and swallowing, leading to life-threatening complications.<\/p>\n

Evrysdi is an oral medication that works by increasing the production of survival motor neuron (SMN) protein, which is crucial for the proper functioning of motor neurons. By increasing SMN protein levels, Evrysdi helps to improve motor function and delay disease progression in infants with SMA.<\/p>\n

The approval of Evrysdi by the European Commission was based on positive results from two clinical trials, FIREFISH and SUNFISH. The FIREFISH trial included infants aged 2 to 7 months with Type 1 SMA, the most severe form of the disease. The study demonstrated that treatment with Evrysdi led to significant improvements in motor function, with many infants achieving milestones such as sitting without support. The SUNFISH trial included children and young adults aged 2 to 25 years with Type 2 or 3 SMA. Results from this study showed that Evrysdi improved motor function compared to a placebo.<\/p>\n

The approval of Evrysdi provides a much-needed treatment option for infants with SMA, particularly those with Type 1 SMA who have historically had limited treatment options. Previously, the only approved treatment for SMA was Spinraza, an injectable medication that requires a lumbar puncture procedure. Evrysdi offers a more convenient and less invasive treatment option, as it can be taken orally.<\/p>\n

The availability of Evrysdi in Europe is expected to have a significant impact on the lives of infants with SMA and their families. By improving motor function and delaying disease progression, Evrysdi can help infants with SMA achieve important developmental milestones and improve their quality of life. Additionally, the oral administration of Evrysdi makes it easier for parents to administer the medication to their infants, reducing the burden of frequent hospital visits.<\/p>\n

Roche’s commitment to developing innovative treatments for rare diseases like SMA is commendable. The approval of Evrysdi by the European Commission is a testament to the company’s dedication to improving the lives of patients with SMA. With this approval, Roche has taken a significant step forward in addressing the unmet medical needs of infants with SMA and providing hope for a brighter future.<\/p>\n

In conclusion, the approval of Roche’s Evrysdi by the European Commission for the treatment of spinal muscular atrophy in infants is a significant development in the field of rare diseases. This oral medication offers a more convenient and less invasive treatment option for infants with SMA, improving motor function and delaying disease progression. The availability of Evrysdi in Europe provides new hope for infants and their families, offering the potential for improved quality of life and developmental outcomes. Roche’s commitment to developing innovative treatments for rare diseases is commendable, and this approval marks an important milestone in the fight against SMA.<\/p>\n