Design and Estimation for Evaluating Principal Surrogate Markers in Vaccine Trials
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Publication:2846433
DOI10.1111/BIOM.12014zbMath1274.62794OpenAlexW2157475378WikidataQ39467318 ScholiaQ39467318MaRDI QIDQ2846433
Julian Wolfson, Ying Huang, Peter B. Gilbert
Publication date: 5 September 2013
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: http://europepmc.org/articles/pmc3713795
two-phase sampling designpseudo-scoreestimated likelihoodprincipal surrogatecloseout placebo vaccinationimmune correlate
Related Items (4)
Sensitivity analysis for evaluating principal surrogate endpoints relaxing the equal early clinical risk assumption ⋮ A unified evaluation of differential vaccine efficacy ⋮ Predicting overall vaccine efficacy in a new setting by re-calibrating baseline covariate and intermediate response endpoint effect modifiers of type-specific vaccine efficacy ⋮ Evaluating principal surrogate markers in vaccine trials in the presence of multiphase sampling
Cites Work
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- Statistical Identifiability and the Surrogate Endpoint Problem, with Application to Vaccine Trials
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- Related Causal Frameworks for Surrogate Outcomes
- A Pseudoscore Estimator for Regression Problems With Two-Phase Sampling
- The validation of surrogate endpoints in meta-analyses of randomized experiments
- Augmented Designs to Assess Immune Response in Vaccine Trials
- A Generalization of Sampling Without Replacement From a Finite Universe
- Assessing Vaccine Effects in Repeated Low‐Dose Challenge Experiments
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