Method for evaluating the human bioequivalence of acarbose based on pharmacodynamic parameters

OBJECTIVE: To explore a method for evaluating the bioequivalence of acarbose based on pharmacodynamic parameters using a single-dose, randomized-sequence, three-way crossover study of acarbose test (T) and reference (R) formulations. METHODS: Baseline-adjusted, pre-dose value deduction, and direct c...

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Detalles Bibliográficos
Autores principales: Xu, Su-Mei, Xu, Yu-Ying, Yan, Juan, Zhang, Yi-Fei, Li, Dai, Li, Dan, Li, Xiao-Min, Guo, Jie, Xu, Ping-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Pre-Clinical Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556174/
https://www.ncbi.nlm.nih.gov/pubmed/33044102
http://dx.doi.org/10.1177/0300060520960317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556174/
https://www.ncbi.nlm.nih.gov/pubmed/33044102
http://dx.doi.org/10.1177/0300060520960317

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