FDA and EMA end points: which outcome end points should we use in clinical trials in patients with irritable bowel syndrome?

Volume: 25, Issue: 6, Pages: 453 - 457
Published: May 14, 2013
Abstract
Trial design and endpoints for the evaluation of drug efficacy in irritable bowel syndrome (IBS) underwent major changes over the last two decades. A systematic review in the early 1990s concluded that there were few well-designed and well-executed treatment trials in IBS. Over the next decade, the so-called binary endpoints were used in several clinical trials in IBS in the US, Europe and other parts of the world. In 2006, the Food and Drug...
Paper Details
Title
FDA and EMA end points: which outcome end points should we use in clinical trials in patients with irritable bowel syndrome?
Published Date
May 14, 2013
Volume
25
Issue
6
Pages
453 - 457
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