Principal surrogates in context of high vaccine efficacy
Author:
Affiliation:
1. Statistics , GSK Vaccines , Rixensart , Belgium
2. National Institute of Allergy and Infectious , Rockville , USA
Abstract
Publisher
Walter de Gruyter GmbH
Link
https://www.degruyter.com/document/doi/10.1515/scid-2020-0003/pdf
Reference28 articles.
1. Alonso, A., W. Van der Elst, G. Molenberghs, M. Buyse, and T. Burzykowski. 2015. “On the Relationship between the Causal-Inference and Meta-Analytic Paradigms for the Validation of Surrogate Endpoints.” Biometrics 71: 15–24. https://doi.org/10.1111/biom.12245.
2. Black, S., H. Shinefield, B. Fireman, E. Lewis, P. Ray, J. R. Hansen, L. Elvin, K. M. Ensor, J. Hackell, G. Siber, F. Malinoski, D. Madore, I. Chang, R. Kohberger, W. Watson, R. Austrian, and K. Edwards. 2000. “Efficacy, Safety and Immunogenicity of Heptavalent Pneumococcal Conjugate Vaccine in Children.” The Pediatric Infectious Disease Journal 19 (3): 187–95. https://doi.org/10.1097/00006454-200003000-00003.
3. Burzykowski, T., G. Molenberghs, and M. Buyse. 2005. The Evaluation of Surrogate Endpoints. New York: Springer.
4. Buyse, M., G. Molenberghs, T. Burzykowski, D. Renard, and H. Geys. 2000. “The Validation of Surrogate Endpoints in Meta-Analyses of Randomized Experiments.” Biostatistics 1: 49–67. https://doi.org/10.1093/biostatistics/1.1.49.
5. Callegaro, A., and F. Tibaldi. 2019. “Assessing Correlates of Protection in Vaccine Trials: Statistical Solutions in the Context of High Vaccine Efficacy.” BMC Medical Research Methodology 19: 47. https://doi.org/10.1186/s12874-019-0687-y.
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