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Alglucosidase alfa

In 2006 recombinant alglucosidase alfa (Myozyme ) received approval in the United States and Europe for the treatment of Pompe disease in all patients. While the development program of alglucosidase alfa was in consideration of the ICH S6 document, and with further consideration to conduct studies in the most relevant species with the greatest predictability, additional pressure was placed on this program for the establishment of safety in animal studies. [Pg.531]

Myozyme (alglucosidase alfa) (US) Approval 2006 Alglucosidase alfa enzyme replacement therapy Pompe disease... [Pg.948]

See other pages where Alglucosidase alfa is mentioned: [Pg.581]    [Pg.620]    [Pg.507]    [Pg.511]    [Pg.511]    [Pg.512]    [Pg.583]    [Pg.623]    [Pg.57]    [Pg.56]    [Pg.66]    [Pg.17]    [Pg.18]    [Pg.634]    [Pg.665]    [Pg.56]    [Pg.66]   
See also in sourсe #XX -- [ Pg.507 , Pg.511 ]

See also in sourсe #XX -- [ Pg.66 ]

See also in sourсe #XX -- [ Pg.66 ]

See also in sourсe #XX -- [ Pg.66 ]



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