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FDA approves new weekly Leqembi injection for early Alzheimer's, set to launch October 6.
The FDA has approved the subcutaneous autoinjector version of Leqembi, a treatment for early Alzheimer's disease, for maintenance dosing.
This weekly injection, available starting October 6, 2025, aims to slow disease progression in patients with mild cognitive impairment or mild dementia.
The treatment targets amyloid plaque and protofibrils, aiming to maintain patients' cognitive abilities for longer.
The new format reduces the need for IV infusions and their associated healthcare resources, potentially increasing access for new patients.
Safety studies showed similar outcomes to IV treatments but with fewer systemic reactions.
La FDA aprueba una nueva inyección semanal de Leqembi para la enfermedad de Alzheimer temprana, programada para lanzarse el 6 de octubre.