Zogenix Reports Fourth Quarter And Full Year 2010 Financial Results
Provides 2011 Top-line Guidance
Conference Call and Webcast Today, March 3 rd, at 4:30 p.m. EST
SUMAVEL ® DosePro™ 2010 Adoption Highlights
- Fourth quarter 2010 net product revenue up 27% over third quarter 2010
- More than 35,200 SUMAVEL DosePro prescriptions were filled from launch through December 31, 2010, representing approximately 248,200 units*
- 35% of over 7,500 SUMAVEL DosePro prescribers had not written for needle-based injectable sumatriptan during 2010 demonstrating appeal of SUMAVEL DosePro beyond traditional users of sumatriptan injection
- Refill rate for SUMAVEL DosePro at the end of June was 21% and has grown to just under 34% through end of December
- 35% of patients are using SUMAVEL DosePro as part of dual-therapy treatment program
- Completed enrollment of ZX002 Phase 3 safety and efficacy trials - potential to be first FDA approved single-entity, oral controlled-release hydrocodone product
- E.U. marketing authorizations of SUMAVEL DosePro obtained by European commercialization partner Desitin Pharmaceuticals GmbH
- Positive SUMAVEL DosePro Phase 4 results on patient satisfaction and other endpoints presented at AAN in April
- ZX002 top-line Phase 3 efficacy results expected in the third quarter 2011
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