Xeris Pharmaceuticals (NSDQ:XERS) said today that the FDA accepted its new drug application for a ready-to-use liquid glucagon rescue pen device.
The company’s product is designed to treat severe hypoglycemia in people with diabetes. The FDA is slated to make a decision about Xeris’ pen by June 10, 2019.
Get the full story at our sister site, Drug Delivery Business News.
The post FDA to review Xeris’ glucagon rescue pen auto-injector appeared first on MassDevice.
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