Everolimus product-specific bioequivalence guidance

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Current version

Adopted guideline

Reference numberEMA/CHMP/151597/2015
Published03/01/2017
Effective from01/07/2017
KeywordsBioequivalence, generics, everolimus
DescriptionThis document provides product-specific guidance on the demonstration of the bioequivalence of everolimus.
Abbreviations
  • BCS Classification: Biopharmaceutics Classification System
  • AUC0-t: area under the plasma concentration curve from administration to last observed concentration at time t
  • AUC0-72: area under the plasma concentration curve from administration to last observed concentration at 72 hours
  • Cmax: maximum plasma concentration


Document history

First version
Current version

Adopted guideline

 

Overview of comments

 

Draft guideline

Published: 03/01/2017

 

Published: 03/01/2017

 

Published: 02/05/2016

 

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