Pharmacokinetically guided optimum adaptive dose selection in early phase clinical trials (Q1654244): Difference between revisions

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+Patient‐Specific Dose Finding Based on Bivariate Outcomes and Covariates
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+A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
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+Bayesian Analysis of Linear and Non-Linear Population Models by Using the Gibbs Sampler
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+Implementation of a Bayesian Design in a Dose‐Escalation Study of an Experimental Agent in Healthy Volunteers
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