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Zogenix Reports FDA Provides New PDUFA Date for Sumavel(TM) DosePro(TM)
Date:2/18/2009

ith the FDA to help make this important alternative treatment available to patients who suffer from migraines," said Roger L. Hawley, Chief Executive Officer of Zogenix. "We are building commercial inventory and our launch plans are in place. It is our intention to launch the product following FDA approval in the second half of 2009."

About Zogenix

Zogenix, Inc., with offices in Emeryville and San Diego, Calif., is a private, specialty pharmaceutical company with two proprietary product candidates in late-stage development for the treatment of central nervous system disorders and pain. The company's lead product candidate, Sumavel DosePro, enables needle-free subcutaneous delivery of sumatriptan for the treatment of acute migraine and cluster headache. Zogenix submitted a New Drug Application with the U.S. Food and Drug Administration for Sumavel DosePro in December 2007. The company also plans to license the patented DosePro needle- free drug delivery system to other companies. The company's second product candidate, ZX002, is a novel, oral controlled release formulation of hydrocodone for the treatment of chronic pain. This product candidate has completed Phase 2 clinical trials and is ready to begin Phase 3. For additional information, visit http://www.zogenix.com.

Zogenix(TM), Sumavel(TM), and DosePro(TM) are trademarks of Zogenix, Inc.


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