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Neumora Therapeutics reports promising Phase 1b results for NMRA-511, reducing Alzheimer’s-related agitation by 15.7 points on average with no serious side effects.
Neumora Therapeutics reported positive Phase 1b results for NMRA-511, an oral vasopressin 1a receptor antagonist, in adults with Alzheimer’s-related agitation.
The drug showed a 15.7-point reduction in agitation symptoms on the CMAI scale, with stronger effects in patients with higher baseline anxiety, and was well-tolerated with no sedation or serious adverse events.
The company plans to advance to higher-dose trials in 2026 and continue development despite the study’s early stage.
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Neumora Therapeutics informa de resultados prometedores de la Fase 1b para NMRA-511, reduciendo la agitación relacionada con la enfermedad de Alzheimer en un promedio de 15,7 puntos sin efectos secundarios graves.