Zogenix Reports Second Quarter 2012 Financial Results
Reiterates 2012 Financial Guidance
Conference Call and Webcast Today, August 8th, at 4:30 p.m. ET
SUMAVEL ® DosePro ® (sumatriptan injection) Second Quarter 2012 Highlights
- Successfully retained prescribers called on by the Zogenix sales force, increasing their total prescriptions by 6% over the first quarter 2012*
- Generated more than 20,000 total prescriptions in the second quarter, the first period without the primary care co-promotion efforts of Astellas, down 6% from the first quarter 2012*
- Entered exclusive co-promotion agreement with Mallinckrodt LLC (Covidien) with their pain management sales force on track to begin promoting SUMAVEL DosePro to a specified list of high prescribers of triptans in late August
- Continued strong refill rate for SUMAVEL DosePro at 43% from 39% in the previous quarter*
- The FDA accepted for review the New Drug Application (NDA) for Zohydro™ ER (hydrocodone bitartrate extended-release capsules) providing a PDUFA date of March 1, 2013
- Initiated first clinical trial for Relday™ and remain on track to obtain study results by the end of 2012
- Formally launched DosePro® technology co-marketing campaign with Battelle, focused on potential out-licensing opportunities
- Raised net proceeds of $65.5 million in an equity offering, extending cash runway beyond potential Zohydro ER approval and launch
- Repaid $21.2 million for all outstanding loans with Oxford Finance LLC and Silicon Valley Bank resulting in an elimination of approximately $3.5 million per quarter in principal and interest payments
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