Recientemente, la FDA otorgó el estado de Revisión de prioridad a una Solicitud de nuevo fármaco suplementario (sNDA) para zanubrutinib, informa MPR. Si bien el tratamiento, bajo la marca Brukinsa,…
Nosotroscreemos que lospacientes de enfermedadesraras son personas, no undiagnóstico. A través de la educación, conciencia, y unpoco de humor – ayudamospacientes, suscuidadores y simpatizantesbrindándolesnoticias e historiasrelevantesya menudo inspiradoras.
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