Evaluation of the Safety, Tolerability, and Pharmacokinetics of Gammaplex(®) 10% Versus Gammaplex(®) 5% in Subjects with Primary Immunodeficiency

PURPOSE: This phase 3, multicenter, open-label, randomized, two-period, crossover bioequivalence trial evaluated the safety, tolerability, and pharmacokinetics of intravenous immunoglobulins (IVIGs) Gammaplex 5% and Gammaplex 10% in 33 adults and 15 children with primary immunodeficiency diseases (P...

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Detalles Bibliográficos
Autores principales: Wasserman, Richard L., Melamed, Isaac R., Stein, Mark R., Jolles, Stephen, Norton, Miranda, Moy, James N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487756/
https://www.ncbi.nlm.nih.gov/pubmed/28316003
http://dx.doi.org/10.1007/s10875-017-0383-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487756/
https://www.ncbi.nlm.nih.gov/pubmed/28316003
http://dx.doi.org/10.1007/s10875-017-0383-9

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