New data on an injectable form of Eisai’s Alzheimer’s drug Leqembi showed that it was more effective than an intravenous version at clearing amyloid, but also came with a higher risk of brain-related side effects known as ARIA.
The study, which was presented at the Clinical Trials on Alzheimer’s Disease conference in Boston, looked at patients who got weekly subcutaneous injections of Leqembi as an alternative to every-other-week intravenous infusions. The data come from a six-month look at the study, and Eisai aims to submit the formulation for approval once it has a year’s worth of results, by the end of March 2024, according to Michael Irizarry, Eisai’s head of clinical neurology research and deputy chief clinical officer.
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