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Bioequivalence Study of Two Orodispersible Rizatriptan Formulations of 10 mg in Healthy Volunteers

The aim of the study was to assess the bioequivalence and tolerability of two different oral formulations of rizatriptan. A bioequivalence study was carried out in 40 healthy volunteers according to an open label, randomized, two-period, two-sequence, crossover, single dose, and fasting conditions d...

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Detalles Bibliográficos
Autores principales:	Cánovas, Mercè, Polonio, Francisco, Cabré, Francesc
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2016
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064242/ https://www.ncbi.nlm.nih.gov/pubmed/28117317 http://dx.doi.org/10.3390/scipharm84030514

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