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    • Amgen gets USFDA nod...

    Amgen gets USFDA nod to Evenity for treating postmenopausal osteoporosis

    Farhat NasimWritten by Farhat Nasim Published On 2019-04-10T09:55:40+05:30  |  Updated On 10 April 2019 9:55 AM IST
    Amgen gets USFDA nod to Evenity for treating postmenopausal osteoporosis

    Evenity, which belongs to a new class of drugs known as sclerostin inhibitors, is administered with two 105 mg injections every month for a year, followed by chronic therapy with an antiresorptive drug. Amgen said the drug would be launched next week and it will unveil the price of the drug as well.


    New Delhi: The U.S. Food and Drug Administration said on Tuesday it had approved Amgen Inc's osteoporosis treatment for postmenopausal women who are at high risk of fracture.


    Postmenopausal osteoporosis is a chronic condition resulting from progressive bone loss beginning around menopause.


    Read Also: Novartis, Amgen in dispute over Aimovig partnership


    The monthly injection, Evenity, developed jointly with Belgium-based UCB SA, helps reduce the risk of fracture by increasing bone mass and mildly inhibiting the break down of bone minerals.


    Evenity comes with a boxed warning, the FDA's strictest warning, flagging increased risk of heart attack, stroke and cardiovascular-related death.


    The approval is expected to augment sales at Amgen, which faces competition from cheaper rivals for two of its biggest selling products - the white blood cell booster Neulasta and rheumatoid arthritis drug Enbrel.


    Read Also: GE Healthcare announces Digital Collaboration with Amgen


    However, William Blair analyst Matt Phipps expects the initial demand to be slow due to the cardiovascular risks and expects peak sales of $500 million.


    "It's important to carefully select patients for this therapy, which includes avoiding use in patients who have had a heart attack or stroke within the previous year," Hylton Joffe, a director at FDA's Center for Drug Evaluation and Research, said.


    Amgen said the drug would be launched next week and it will unveil the price of the drug as well.


    The decision comes months after an FDA panel overwhelmingly voted for the drug's approval.


    Read Also: Sanofi, Regeneron loses patent challenge to Amgen cholesterol drug Repatha


    Osteoporosis, most common in women who have reached menopause age, affects an estimated 8 million American women.


    The market for such treatment is currently dominated by bone strengthening agents known as antiresorptive therapies, including Merck & Co's Fosamax, which block the normal process of break down of bone minerals. But they take years to get a substantial benefit.


    Evenity, which belongs to a new class of drugs known as sclerostin inhibitors, is administered with two 105 mg injections every month for a year, followed by chronic therapy with an antiresorptive drug.

    Amgenantiresorptive drugantiresorptive therapiesCardiovascularchronic conditionchronic therapydrug EnbrelEvenityFDAFDA approvalfractureheart attackHylton JoffeNeulastaosteoporosis drugosteoporosis treatmentpostmenopausalpostmenopausal osteoporosispostmenopauserheumatoid arthritissclerostin inhibitorsstrokeUCB SAUSFDAWilliam Blair
    Source : Reuters

    Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

    Farhat Nasim
    Farhat Nasim

      Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751 To know about our editorial team click here

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