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Less than four months after the European Medicines Agency recommended in July not to grant marketing authorisation for Leqembi (lecanemab) for the treatment of Alzheimer's disease, the EMA's Committee for Medicinal Products for Human Use (CHMP) has reassessed the available evidence to conclude that the benefits outweigh the risks

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The higher dose of Rybelsus is because oral drugs take longer to enter the bloodstream, giving them lower bioavailability