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FDA approves at-home Alzheimer's drug LEQEMBI for self-administration via weekly injection.
The FDA has approved LEQEMBI IQLIK for at-home treatment of early Alzheimer's disease, allowing patients to administer the drug via a weekly autoinjector after an initial 18-month intravenous treatment.
This marks the first anti-amyloid treatment available for at-home use, providing patients and caregivers with more treatment flexibility.
The drug is set to launch on October 6, 2025.
Clinical trials showed the treatment maintained benefits similar to intravenous methods with no significant adverse events.
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La FDA aprueba el medicamento para la enfermedad de Alzheimer LEQEMBI para autoadministración mediante inyección semanal.