Pharming Group recibe evaluación acelerada en Europa para leniolisib para el tratamiento de inmunodeficiencias raras, APDS ...Middle East

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Pharming Group recibe evaluación acelerada en Europa para leniolisib para el tratamiento de inmunodeficiencias raras, APDS
source : PR Newswire ( Middle East ) () 61
La evaluación acelerada de EMA permite un período de revisión más corto para leniolisib de un estándar de 210 días a 150 días Pharming está en camino de presentar su solicitud de autorización de comercialización para leniolisib en el segundo semestre de 2022 LEIDEN, Países Bajos, 1 de...

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