FDA approves $2.1 million Novartis' 'Zolgensma', makes it the costliest drug ever
Zolgensma, a one-time drug for spinal muscular atrophy, affects 1 in 10,000 children and mostly leads to death.


Representational image. Image credit: Reuters[/caption]Zolgensma works by providing a functional copy of the defective gene responsible for SMA to halt the disease's progression via a one-time intravenous infusion. The US Food and Drug Administration said the drug's safety had been tested in an ongoing clinical trial and a completed clinical trial involving 36 patients between the ages of two weeks and eight months.Most of the evidence of its effectiveness was based on the results of the ongoing trial, which found that "patients treated with Zolgensma... demonstrated significant improvement in their ability to reach developmental motor milestones" including head control and the ability to sit without support.Jerry Mendell, a doctor involved in the trial at Nationwide Children's Hospital in Columbus, Ohio, added that the "level of efficacy, delivered as a single, one-time therapy, is truly remarkable and provides a level of unprecedented hope for families."The most common side effects of Zolgensma are elevated liver enzymes and vomiting, the FDA said. Gene and cell therapies leverage the biology to reverse diseases ranging from congenital blindness to pediatric leukemia.

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