Optimal Timing for Interim Analyses in Clinical Trials
Author:
Affiliation:
1. a Clinical Statistics, Pfizer Japan, Inc. , Tokyo , Japan
2. b Science and Technology , Seikei University , Tokyo , Japan
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1080/10543406.2013.813522
Reference14 articles.
1. Increasing the sample size when the unblinded interim result is promising
2. Two-Stage Plans Compared with Fixed-Sample-Size and Wald SPRT Plans
3. Modification of Sample Size in Group Sequential Clinical Trials
4. The need for more efficient trial designs
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