ICH guideline

ICH E20 EWG: Adaptive Designs for Clinical Trials

ICH guideline · Efficacy Guidelines · Step 3

Key facts

ICH code E20 EWG
Title Adaptive Designs for Clinical Trials
Guideline series Efficacy Guidelines
ICH step Step 3
ICH summary (excerpt) This topic was endorsed by the ICH Assembly in June 2018. The E20 EWG is working on the development of a new E20 Guideline on “Adaptive Clinical Trials” on the design, conduct, analysis, and interpretation of adaptive clinical trials that provides a transparent and harmonized set of principles for the regulatory review…
File E20 Step 2 Presentation
File type PDF
File on ich.org database.ich.org

At a glance

  • Yes Full text searchable in Orca1
  • E20 Step 2 Presentation Files published by ICH
  • None FDA guidance documents based on this guideline

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ICH guidelines

ICH guidelines harmonise the technical requirements for registering medicines in the ICH regions. Each guideline moves through a five-step process, from concept paper to adoption and implementation by regulators.

Source: International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). Guideline summaries are ICH material, reproduced with acknowledgement

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