La vacuna Sputnik V tuvo un 91,4% de eficacia en 22 mil voluntarios. Surge del an\u00e1lisis final de los datos obtenidos 21 d\u00edas despu\u00e9s de la administraci\u00f3n de la primera dosis.<\/p>\n
\n
El Centro Gamaleya, que desarrolla la vacuna rusa Sputnik V, asegur\u00f3 este lunes que logr\u00f3 alcanzar una eficacia contra el coronavirus del 91,4% y destac\u00f3 la importancia del contrato firmado con la Argentina para recibir el medicamento.<\/p>\n
\u201cLa eficacia de la vacuna es del 91,4%, seg\u00fan el an\u00e1lisis final del punto de control de los datos obtenidos 21 d\u00edas despu\u00e9s de la administraci\u00f3n de la primera dosis\u201d, se\u00f1al\u00f3 el Centro Gamaleya en un comunicado.<\/p>\n
Durante una conferencia de prensa virtual, su titular, Kiril Dmitreiv, destac\u00f3 como uno de los logros del centro el acuerdo firmado con la Argentina para recibir la vacuna, y explic\u00f3 que en los pr\u00f3ximos d\u00edas los resultados de los ensayos cl\u00ednicos ser\u00e1n publicados en la revista cient\u00edfica Lancet.<\/p>\n
De acuerdo con el protocolo de los ensayos cl\u00ednicos de fase 3, la eficacia provisional se calcula en base a tres puntos de control estad\u00edsticamente significativos: al alcanzar los 20, 39 y 78 casos de la nueva infecci\u00f3n por coronavirus entre los sujetos del grupo placebo y del grupo que recibi\u00f3 la vacuna.<\/p>\n
En el primer an\u00e1lisis provisional (al alcanzar los 20 casos), la vacuna demostr\u00f3 una eficacia del 92%. En el segundo an\u00e1lisis provisional (39 casos) la eficacia fue del 91,4%. El tercer y \u00faltimo an\u00e1lisis de datos provisionales (que se present\u00f3 este lunes) se llev\u00f3 a cabo tras alcanzar los 78 casos de coronavirus entre los participantes del estudio.<\/p>\n
Demostr\u00f3 que\u00a0la eficacia de la vacuna Sputnik V es del 91,4%, seg\u00fan los datos obtenidos 21 d\u00edas despu\u00e9s de la administraci\u00f3n de la primera dosis.\u00a0El c\u00e1lculo se bas\u00f3 en\u00a022.714 voluntarios\u00a0que recibieron tanto la primera como la segunda dosis.<\/p>\n
No se identificaron, adem\u00e1s, \u00a0eventos adversos\u00a0inesperados como parte de la investigaci\u00f3n, seg\u00fan el comunicado. Y agrega que las condiciones de salud de los participantes ser\u00e1n monitoreadas durante al menos seis meses despu\u00e9s de recibir la primera vacuna.<\/p>\n
Cabe recordar que el presidente Alberto Fern\u00e1ndez anunci\u00f3 la semana pasada que la Argentina firm\u00f3 con Rusia el acuerdo para el arribo al pa\u00eds de la vacuna Sputnik V contra el coronavirus. Confirm\u00f3 que antes de fin de a\u00f1o llegar\u00e1n 600 mil dosis, con lo que se podr\u00e1 vacunar a 300 mil personas. Adem\u00e1s, entre enero y febrero arribar\u00e1n otras 20 millones de dosis.<\/p>\n
Fuente: DIB<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"
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