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    • Novartis plans gene...

    Novartis plans gene therapy price lower than $4 million to $5 million range

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2019-05-23T09:00:07+05:30  |  Updated On 23 May 2019 9:00 AM IST
    Novartis plans gene therapy price lower than $4 million to $5 million range

    Novartis has previously said it could price the treatment in a range of $1.5 million to $5 million.


    BOSTON: Novartis AG's top executive said on Wednesday it expects to price its gene therapy for spinal muscular atrophy "far lower" than the $4 million to $5 million figure the Swiss drugmaker has said it could be worth.


    U.S. regulators are expected to make a decision this month on whether to approve Zolgensma, a one-time therapy seen as a potential long-term solution for the rare disease that is the leading genetic cause of death in infants. The company has previously said it could price the treatment in a range of $1.5 million to $5 million.


    Read Also: Japan: Novartis gets Government nod for cancer treatment Kymriah at cost of $305800


    "We won't be announcing the price until we get the approval. But our overall goal is to be at a fraction of what is the current standard of care, and the current standard of care for treating these patients is $4 million to $5 million over 10 years," Novartis Chief Executive Vas Narasimhan told reporters on Wednesday in Boston.


    The current treatment for SMA, which can lead to paralysis, breathing difficulty and early death, is Biogen Inc's Spinoza. That drug has a list price of $750,000 for the initial year and $375,000 annually thereafter.


    Read Also: Novartis recalls three lots of Promacta due to potential peanut contamination


    Narasimhan said his company's ultra-rare disease therapy would be cost-effective in a range of $4.6 million to $5.4 million. "We want to be far lower than that," he said.


    Novartis is expecting the drug initially to be approved for infants and is in discussions with the U.S. Food and Drug Administration about whether approval will include other forms of the disease beyond the most serious Type 1, he said.


    Read Also: Novartis to fight US price-fixing claims against Sandoz unit


    The company is also in late-stage discussions with commercial insurers over the price of the treatment.

    atrophyBiogenBostongene therapyinfants deathNovartisNovartis CEONovartis chief executivespinal muscular atrophySpinozaSwiss drugmakertreatmentUS Food and Drug AdministrationUSFDAVas NarasimhanZolgensmaZolgensma price
    Source : Reuters

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    Medical Dialogues Bureau
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      Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in. Check out more about our bureau/team here

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