EMA explains when to use active controls in clinical trials

This article was originally published in SRA

12 Jan 2011
News

Vibha Sharma @ScripRegVibha vibha.sharma@informa.com

Executive Summary

The European Medicines Agency has issued a draft reflection paper explaining when drug companies should make use of active control in clinical trials. The scope of the paper is restricted to therapeutic areas where the use of a placebo is deemed ethical and one or more established medicines are available¹^,2.

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EMA explains when to use active controls in clinical trials

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