Sample Size Re-Estimation without Breaking the Blind in Clinical Trial
Author:
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference11 articles.
1. Biostatistical methodology in clinical trials in applications for marketing authorizations for medicinal products. CPMP working party on efficacy of medicinal products note for guidance III/3630/92-EN
2. Sample Size Recalculation in Internal Pilot Study Designs: A Review
3. Sample size re-estimation without unblinding for normally distributed outcomes with unknown variance
4. Understanding the FDA Guidance on Adaptive Designs: Historical, Legal, and Statistical Perspectives
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3. Adaptive clinical endpoint bioequivalence studies with sample size re-estimation based on a nuisance parameter;Journal of Biopharmaceutical Statistics;2019-09-03
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