Zogenix Licenses European Development and Commercial Rights for sumatriptan DosePro(TM) to Desitin Pharmaceuticals, GmbH



    Zogenix, Inc. ("Zogenix"), a private, specialty pharmaceutical
    company, today announced that it has entered into a license agreement
    to grant exclusive rights in the European Union to Desitin
    Pharmaceuticals, GmbH ("Desitin") to develop and commercialize
    Zogenix´s late stage, single use, needle-free product candidate for
    migraine headache, sumatriptan DosePro. The product candidate, that
    incorporates the Zogenix DosePro needle-free drug delivery technology,
    has previously demonstrated bioequivalence to the Imitrex STATdose
    System(R) (sumatriptan injection, GlaxoSmithKline) in a U.S. pivotal
    clinical trial and compelling ease-of-use in a usability trial with
    migraine sufferers.

    Under the terms of the agreement, Desitin will oversee, and be
    responsible for the expenses related to, all clinical development,
    regulatory approvals and commercialization efforts required to market
    and sell sumatriptan DosePro across Europe. Zogenix will be
    responsible for the manufacture and supply of commercial product, and
    will receive a transfer price payment on manufactured product and
    royalty payments based on sales of the product upon commercialization.
    Zogenix retains full commercial rights to sumatriptan DosePro in the
    U.S., Canada, Asia and certain other countries.

    Sales of triptans, the class of drugs in which sumatriptan DosePro
    is expected to compete, total approximately $550 million annually in
    the five major countries of Europe: Germany, France, Italy, Spain, and
    the UK, according to IMS Health MIDAS. "Triptans remain the standard
    of care in migraine treatment," commented Dr. Stephen Farr, President
    and Chief Operating Officer of Zogenix. "However, there remains a
    significant unmet medical need for more effective, easy-to-use
    triptans that can deliver on the promise of providing faster onset and
    more complete pain relief without the use of a needle. Sumatriptan
    DosePro is designed to meet these needs."

    "This license agreement expands the potential reach for
    sumatriptan DosePro beyond the U.S., where, subject to regulatory
    approval, Zogenix is preparing to commercialize sumatriptan DosePro
    ourselves," said Roger Hawley, Chief Executive Officer of Zogenix. "In
    Desitin, we have chosen a European partner that has a proven track
    record of successfully developing, registering and commercializing
    central nervous system (CNS) products. We look forward to seeing
    sumatriptan DosePro advance through these steps and launch in the
    European marketplace."

    "This agreement reflects the unique and well respected position
    Desitin holds in the European CNS market. We have the ability to both
    move this product candidate through the European regulatory process
    and to launch it with our CNS-focused sales representatives in more
    than nine countries," commented Dr. Martin Zentgraf, Desitin´s General
    Manager. "This product candidate fits with our ongoing commitment to
    develop improved products that address unmet medical needs in the CNS
    market. We are delighted to be working with Zogenix and, subject to
    regulatory approval, look forward to bringing this important product
    candidate to the market for the benefit of patients."

    About Zogenix

    Zogenix, Inc., with offices in Emeryville and San Diego, CA, 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, sumatriptan DosePro (previously Intraject(R)), enables
    needle-free subcutaneous delivery of sumatriptan for the treatment of
    acute migraine. In December 2007, Zogenix submitted a New Drug
    Application with the U.S. Food and Drug Administration for sumatriptan
    DosePro. Zogenix´s second product candidate, ZX002, is a novel
    controlled release formulation of hydrocodone for the treatment of
    chronic pain. This product candidate has completed Phase 2 clinical
    trials, and the company anticipates initiating the Phase 3 clinical
    program in the second half of 2008. The company also plans to license
    the patented DosePro drug delivery system to other companies. For
    additional information, visit www.zogenix.com.

    About Desitin

    Desitin Arzneimittel GmbH, based in Hamburg, Germany is an
    independent, private, fully integrated, German pharmaceutical company
    focused on the development, manufacturing and distribution of products
    for the treatment of central nervous system disorders. Desitin, with
    turnover in 2005/2006 of over $100 million, is one of the leading
    European companies in the field of epilepsy with additional expertise
    in Parkinson´s disease and psychiatric disorders. With their
    pharmaceutical and clinical development capabilities, the company
    develops innovative products such as controlled-release and high-dose
    antiepileptics. Desitin´s sales infrastructure offers comprehensive
    coverage in Germany, Northern and Eastern Europe. The company also has
    strategic partnerships with other companies covering nearly all of the
    remaining countries in Europe. For additional information, visit
    www.desitinpharma.com

    Bourne Partners, Charlotte N.C., acted as financial advisors to
    Desitin on this transaction.

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

    Imitrex STATdose System(R) is a registered trademark of
    GlaxoSmithKline.