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  "Title": "Simulate, Evaluate, and Analyze Dose Finding Trials with\nBayesian MCPMod",
  "Version": "1.3.2",
  "Authors@R": "c(\nperson(\"Boehringer Ingelheim Pharma GmbH & Co. KG\", role = c(\"cph\", \"fnd\")),\nperson(\"Stephan\", \"Wojciekowski\", , \"stephan.wojciekowski@boehringer-ingelheim.com\", role = c(\"aut\", \"cre\")),\nperson(\"Lars\", \"Andersen\", , \"lars.andersen@boehringer-ingelheim.com\", role = \"aut\"),\nperson(\"Jonas\", \"Schick\", , \"jonas.schick@boehringer-ingelheim.com\", role = \"ctb\"),\nperson(\"Sebastian\", \"Bossert\", , \"sebastian.bossert@boehringer-ingelheim.com\", role = \"aut\")\n)",
  "Description": "Bayesian MCPMod (Fleischer et al. (2022)\n<doi:10.1002/pst.2193>) is an innovative method that improves\nthe traditional MCPMod by systematically incorporating\nhistorical data, such as previous placebo group data. This\npackage offers functions for simulating, analyzing, and\nevaluating Bayesian MCPMod trials with normally and binary\ndistributed endpoints. It enables the assessment of trial\ndesigns incorporating historical data across various true\ndose-response relationships and sample sizes. Robust mixture\nprior distributions, such as those derived with the\nMeta-Analytic-Predictive approach (Schmidli et al. (2014)\n<doi:10.1111/biom.12242>), can be specified for each dose\ngroup.  Resulting mixture posterior distributions are used in\nthe Bayesian Multiple Comparison Procedure and modeling steps.\nThe modeling step also includes a weighted model averaging\napproach (Pinheiro et al. (2014) <doi:10.1002/sim.6052>).\nEstimated dose-response relationships can be bootstrapped and\nvisualized.",
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