On “Re‐randomization tests as sensitivity analyses to confirm immunological noninferiority of an investigational vaccine: Case study” by Luca Grassano et al. (2023, Pharmaceutical Statistics)
Author:
Affiliation:
1. Novartis Pharmaceuticals Corporation East Hanover New Jersey USA
2. National Institutes of Health Bethesda Maryland USA
3. Boehringer Ingelheim Pharmaceuticals Inc. Ridgefield Connecticut USA
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pst.2363
Reference14 articles.
1. Re‐randomization tests as sensitivity analyses to confirm immunological noninferiority of an investigational vaccine: Case study
2. Sequential Treatment Assignment with Balancing for Prognostic Factors in the Controlled Clinical Trial
3. Minimization: A new method of assigning patients to treatment and control groups
4. FDA Guidance for Industry.Adaptive Designs for Clinical Trials of Drugs and Biologics. November 2019.https://www.fda.gov/media/78495/download
5. EMA Guideline on Adjustment for Baseline Covariates in Clinical Trials. 26 February 2015.https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-adjustment-baseline-covariates-clinical-trials_en.pdf
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