Video Experimental Relacionado
Updated: Feb 20, 2026

10:30
Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
Published on: May 24, 2016
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Un conjugado anticuerpo-oligonucleótido para la distrofia miotónica tipo 1
Nicholas E Johnson1, Li-Jung Tai2, Johanna I Hamel3
1Virginia Commonwealth University, Richmond.
The New England journal of medicine
|February 18, 2026
Resumen
Delpacibart etedesiran (del-desiran) muestra promesa en el tratamiento de la distrofia miotónica tipo 1 al reducir el ARNm tóxico y mejorar los patrones de empalme. Se justifica una mayor investigación clínica a pesar de algunos eventos adversos graves observados.
Conclusiones:
- Del-desiran demostró la entrega muscular y la mejora del empalme aberrante en pacientes con DM1.
- El perfil de seguridad y la eficacia observados respaldan una mayor investigación clínica de del-desiran.
- Se observaron dos eventos adversos graves, lo que justifica una monitorización cuidadosa en futuros ensayos.
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