CoLucid (NASDAQ: CLCD) is a Phase 3 clinical-stage biopharmaceutical company that is developing an innovative and proprietary small molecule for the acute treatment of migraine headaches. The Company’s lead product candidate, lasmiditan, utilizes the first new mechanism of action for acute treatment of migraine in the last twenty years, and has the potential to address the unmet needs of migraine patients, including those with cardiovascular risk factors or stable cardiovascular disease, and those who are dissatisfied with existing therapies. According to the American Migraine Foundation, migraine affects 12% of the population in the United States and is the leading cause of disability among neurological disorders in the United States. The direct and indirect costs of migraine in the United States are estimated at over $20 billion annually. Over 500 patients to date have been dosed with lasmiditan. In a Phase 2b clinical trial of the compound, the primary endpoint of headache relief was met with statistical significance, as were the secondary endpoints of freedom from the associated symptoms of nausea, and sensitivity to sound and sensitivity to light. CoLucid has completed the first pivotal Phase 3 randomized, double-blind, placebo-controlled clinical trial of lasmiditan, or SAMURAI, under a special protocol assessment (SPA) agreement with the FDA. See press release for top line data.
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NASDAQ CLCD (Common Stock)
02/22/17 4:00 p.m. ET
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News & Events
November 14, 2016
CoLucid Pharmaceuticals Provides SPARTAN Enrollment Update