Incorporating founder virus information in vaccine field trials
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- Peter B. Gilbert & Bryan E. Shepherd & Michael G. Hudgens, 2013. "Sensitivity Analysis of Per-Protocol Time-to-Event Treatment Efficacy in Randomized Clinical Trials," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 108(503), pages 789-800, September.
- Devan V. Mehrotra & Xiaoming Li & Peter B. Gilbert, 2006. "A Comparison of Eight Methods for the Dual-Endpoint Evaluation of Efficacy in a Proof-of-Concept HIV Vaccine Trial," Biometrics, The International Biometric Society, vol. 62(3), pages 893-900, September.
- Shepherd, Bryan E. & Gilbert, Peter B. & Lumley, Thomas, 2007. "Sensitivity Analyses Comparing Time-to-Event Outcomes Existing Only in a Subset Selected Postrandomization," Journal of the American Statistical Association, American Statistical Association, vol. 102, pages 573-582, June.
- Dean Follmann, 2006. "Augmented Designs to Assess Immune Response in Vaccine Trials," Biometrics, The International Biometric Society, vol. 62(4), pages 1161-1169, December.
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- Dean Follmann & Chiung‐Yu Huang, 2018. "Sieve analysis using the number of infecting pathogens," Biometrics, The International Biometric Society, vol. 74(3), pages 1023-1033, September.
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