Daiichi Sankyo’s (TYO: 4568) European subsidiary and Esperion Therapeutics (Nasdaq: ESPR) announced that positive results from the 2,230 patient, 52-week, Phase III long-term safety study of bempedoic acid were published in NEJM. The paper can be found online here.
Bempedoic acid is being developed as a convenient, once-daily, oral therapy for the treatment of patients with elevated LDL-C. Bempedoic acid and the bempedoic acid/ezetimibe combination are currently undergoing regulatory review for marketing authorization by the European Medicines Agency. A decision is expected during the first half of 2020.
Esperion granted Daiichi Sankyo exclusive rights to commercialize bempedoic acid and the bempedoic acid/ezetimibe combination pill in the European Economic Area and Switzerland in January this year, in a deal worth a potential $900 million in milestone payments.
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