Surrogate: Evaluation of Surrogate Endpoints in Clinical Trials
In a clinical trial, it frequently occurs that the most credible outcome to evaluate the effectiveness of a new therapy (the true endpoint) is difficult to measure. In such a situation, it can be an effective strategy to replace the true endpoint by a biomarker that is easier to measure and that allows for a prediction of the treatment effect on the true endpoint (a surrogate endpoint). The package 'Surrogate' allows for an evaluation of the appropriateness of a candidate surrogate endpoint based on the meta-analytic, information-theoretic, and causal-inference frameworks. Part of this software has been developed using funding provided from the European Union's 7th Framework Programme for research, technological development and demonstration under Grant Agreement no 602552.
||MASS, nlme, msm, lme4
||Wim Van der Elst, Ariel Alonso & Geert Molenberghs
||Wim Van der Elst <Wim.vanderelst at gmail.com>
||Wim Van der Elst <Wim.email@example.com>
||GPL-2 | GPL-3 [expanded from: GPL (≥ 2)]