Nucala (mepolizumab) Gains FDA Approval for Two New Self-Administration Options
GSK plc American Depositary Shares (Each representing two Ordinary Shares) (GSK)
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Source: Business Wire
First anti-IL5 biologic to give healthcare professionals choice of how and where their patients receive treatment LONDON--(BUSINESS WIRE)-- GlaxoSmithKline (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has approved two new methods for administering Nucala (mepolizumab), an autoinjector and a pre-filled safety syringe, for patients or caregivers to administer once every four weeks, after a healthcare professional decides it is appropriate. This is the first anti-IL5 biologic to be licensed in the US for at-home administration, and the first respiratory biologic to be approved for administration via an autoinjector. This press release features multimedia. View the full release here:https://www.businesswire.com/news/home/20190606005859/en/ Nucala (mepolizumab) Autoinjector (Photo: Business Wire) This approval will give healthcare professionals and people living with severe
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