CAMBRIDGE, Mass., Aug. 10, 2016 (GLOBE NEWSWIRE) -- CoLucid Pharmaceuticals, Inc. (NASDAQ:CLCD) today reported financial and operating results for the quarter ended June 30, 2016.
Corporate Highlights
On June 7, CoLucid announced that the last patient has been randomized in SAMURAI the first Phase 3 pivotal clinical trial for lasmiditan oral tablets (100 mg and 200 mg) for the acute treatment of migraine. The objectives of SAMURAI are to evaluate the safety and efficacy of lasmiditan (100 mg and 200 mg) in comparison to placebo two hours after dosing on freedom from migraine headache pain, which is the primary endpoint, and on freedom from the most bothersome associated symptom of migraine (nausea, phonophobia or photophobia), which is the key secondary endpoint. CoLucid is now working towards database lock and analysis, with SAMURAI top-line data expected to be released during the week of September 5. More detailed results are expected to be presented at a symposium during the 5th European Headache and Migraine Trust International Congress taking place in Glasgow, Scotland on September 17, 2016. SAMURAI is being conducted under a Special Protocol Assessment (“SPA”) agreement with the U.S. Food and Drug Agency (“FDA”).
Corporate Highlights
On June 7, CoLucid announced that the last patient has been randomized in SAMURAI the first Phase 3 pivotal clinical trial for lasmiditan oral tablets (100 mg and 200 mg) for the acute treatment of migraine. The objectives of SAMURAI are to evaluate the safety and efficacy of lasmiditan (100 mg and 200 mg) in comparison to placebo two hours after dosing on freedom from migraine headache pain, which is the primary endpoint, and on freedom from the most bothersome associated symptom of migraine (nausea, phonophobia or photophobia), which is the key secondary endpoint. CoLucid is now working towards database lock and analysis, with SAMURAI top-line data expected to be released during the week of September 5. More detailed results are expected to be presented at a symposium during the 5th European Headache and Migraine Trust International Congress taking place in Glasgow, Scotland on September 17, 2016. SAMURAI is being conducted under a Special Protocol Assessment (“SPA”) agreement with the U.S. Food and Drug Agency (“FDA”).
