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

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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