Agalsidase alfa and agalsidase beta in the treatment of fabry disease: Does the dose really matter?
Academic Article
Publication Date:
2015
abstract:
Agalsidase alfa was well
tolerated throughout the observation period, and no clinical
problem occurred after the reintroduction of agalsidase beta
in patients who switched back. Despite the exiguous number
of patients involved in this observation, and considering that
80% of the patients treated with this drug were males, who
are more prone to disease progression, these data offer further
information about the safety and efficacy of agalsidase alfa.
Iris type:
01.01 Articolo in rivista
Keywords:
fabry disease
List of contributors:
Riccio, Eleonora
Published in: