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FDA accepted our NDA for Sprix™ for full review. A PDUFA date of October 5, 2009 has been set.
Completed a Series B financing that raised $42.7 million.
Completed a Phase 2 clinical study of ROX-828 for the treatment of migraine.
Identify a commercial US partner for Sprix™.
Submit data from our Phase 3 studies of Sprix™ for publication in peer-reviewed scientific journals.