On the efficiency of adaptive sample size design

Author:

Cui Lu1ORCID,Zhang Lanju1ORCID

Affiliation:

1. AbbVie Inc North Chicago Illinois

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

Reference32 articles.

1. U.S. Food & Drug Administration.Adaptive designs for medical device clinical studies. FDA Website.2016.https://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm446729.pdf. Accessed August 28 2018.

2. U.S. Food & Drug Administration.Draft guidance for industry: adaptive design clinical trials for drugs and biologics. FDA Website.2010.https://www.fda.gov/downloads/drugs/guidances/ucm201790.pdf. Accessed August 28 2018.

3. Committee for Medicinal Products for Human Use (CHMP).Reflection paper on methodological issues in confirmatory clinical trials planned with an adaptive design. EMA Website.2007.http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003616.pdf. Accessed August 28 2018.

4. H.R.34—21st Century Cures Act. United States Congress Website.2016.https://www.congress.gov/bill/114th-congress/house-bill/34. Accessed August 28 2018.

5. On the inefficiency of the adaptive design for monitoring clinical trials

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