Statistical Considerations for Testing Multiple Endpoints in Group Sequential or Adaptive Clinical Trials
Author:
Affiliation:
1. a Division of Biometrics I, OB/OTS/CDER, FDA , Silver Spring, Maryland, USA
2. b Office of Biostatistics, OTS/CDER, FDA , Silver Spring, Maryland, USA
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1080/10543400701645405
Reference11 articles.
1. Evaluation of Experiments with Adaptive Interim Analyses
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5. Methodological issues with adaptation of clinical trial design
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