FDA nods Lumizyme

August 5, 2014

LUMIZYME (alglucosidase alfa) for the rare but debilitating enzyme deficiency Pompe disease, has been approved for expanded use to now include patients less than eight years of age by the US Food and Drug Administration (FDA). Lumizyme is marketed in Australia as Myozyme and has been approved by the Therapeutic Goods Administration since 14 Mar 2008. The FDA also approved Jardiance (empagliflozin) tablets, marketed as Ronjoli in Australia, as an addition to diet and exercise to improve glycemic control in adults with type 2 diabetes.

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Pharmacy Daily | FDA nods Lumizyme

FDA nods Lumizyme

Other recent headlines

PD breaking news – Pharmacists to administer NIP vaccinations in aged care

PD breaking news – Top Western Australian talent honoured

Legal action for Montu

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES