Pharmaceutical Business review

FDA accepts Zogenix’s NDA for migraine drug

The FDA will take action on its application in late 2008. Sumatriptan DosePro (formerly known as Intraject sumatriptan) utilizes Zogenix’s proprietary DosePro needle-free drug delivery system to subcutaneously administer sumatriptan.

Roger Hawley, CEO of Zogenix, said: “We are very pleased to have our first new drug application (NDA) accepted for filing by the FDA. In just 18 months, we have progressed from a start-up stage company to one now with our first product under review by the FDA for approval.”