Cargando…
In Vitro–In Vivo Correlation (IVIVC) Population Modeling for the In Silico Bioequivalence of a Long-Acting Release Formulation of Progesterone
Health authorities carefully evaluate any change in the batch manufacturing process of a drug before and after regulatory approval. In the absence of an adequate in vitro–in vivo correlation (Level A IVIVC), an in vivo bioequivalence (BE) study is frequently required, increasing the cost and time of...
Autores principales: | Tosca, Elena M., Rocchetti, Maurizio, Pérez, Elena, Nieto, Conchi, Bettica, Paolo, Moscoso del Prado, Jaime, Magni, Paolo, De Nicolao, Giuseppe |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918143/ https://www.ncbi.nlm.nih.gov/pubmed/33673306 http://dx.doi.org/10.3390/pharmaceutics13020255 |
Ejemplares similares
-
Evaluating the bioequivalence of two pitavastatin calcium formulations based on IVIVC modeling and clinical study
por: Wang, Jiaying, et al.
Publicado: (2022) -
A Dynamic Energy Budget (DEB) based modeling framework to describe tumor-in-host growth inhibition and cachexia onset during anticancer treatment in in vivo xenograft studies
por: Tosca, Elena Maria, et al.
Publicado: (2021) -
IVIVC from Long Acting Olanzapine Microspheres
por: D'Souza, Susan, et al.
Publicado: (2014) -
Evaluation of Bioequivalence of Two Long-Acting 20% Oxytetracycline Formulations in Pigs
por: Lei, Zhixin, et al.
Publicado: (2017) -
Development and validation of an in vitro–in vivo correlation (IVIVC) model for propranolol hydrochloride extended-release matrix formulations
por: Cheng, Chinhwa, et al.
Publicado: (2013)