Biogen and Eisai Co. Ltd. announced a decision on 13 September that seemed inevitable after many failures in the same drug class: the companies said they will discontinue two Phase III clinical trials (MISSION AD1 and AD2) for the beta amyloid cleaving enzyme (BACE) inhibitor elenbecestat in Alzheimer’s disease after a safety review by the data safety monitoring board observed an unfavorable risk-benefit ratio.
Elenbecestat (E2609) was the last BACE inhibitor in clinical development after development of 16 other candidates against this target was suspended for safety and efficacy issues, such as elevated liver enzymes and worsening cognition. These included the Novartis AG and Amgen Inc
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