On optimal designs for clinical trials: an updated review (Q2301225): Difference between revisions

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+Optimum designs for two treatments with unequal variances in the presence of covariates
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+Adaptive Designs to Maximize Power in Clinical Trials with Multiple Treatments
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+Optimal Bayesian-feasible dose escalation for cancer phase I trials
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+A theoretical analysis of the power of biased coin designs
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+Compound optimal allocation for individual and collective ethics in binary clinical trials
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+Compound optimal designs for percentile estimation in dose-response models with restricted design intervals
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+Multi-treatment optimal response-adaptive designs for phase III clinical trials
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+Response-adaptive dose-finding under model uncertainty
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+Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies
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+Optimal Bayesian design applied to logistic regression experiments
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+Bayesian experimental design: A review
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+On multiple-objective optimal designs
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+Locally Optimal Designs for Estimating Parameters
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+Semiparametric Dose Finding Methods
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+The Equivalence of Constrained and Weighted Designs in Multiple Objective Design Problems
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+Invited Discussion Paper Constrained Optimization of Experimental Design
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+On the Equivalence of Constrained and Compound Optimal Designs
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+Optimal Designs for Dose-Finding Studies
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+Optimal designs for the emax, log-linear and exponential models
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+Adaptive designs for dose-finding based on efficacy-toxicity response
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+A Random Walk Rule for Phase I Clinical Trials
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+Using the Canonical Design Space to Obtain c-optimal Designs for the Quadratic Logistic Model
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+Optimal designs and limiting optimal designs for a trinomial response
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+Optimal Design for Nonlinear Response Models
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+Optimal responses-adaptive designs based on efficiency, ethic, and cost
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+Asymptotically Optimal Response‐Adaptive Designs for Allocating the Best Treatment: An Overview
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+Bayesian Optimal Designs for Phase I Clinical Trials
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+Optimal Designs for Bivariate Logistic Regression
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+The Theory of Response‐Adaptive Randomization in Clinical Trials
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+D-optimal designs for logistic models with three and four parameters
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+Optimal designs for binary data under logistic regression
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+Optimal designs for contingent response models with application to toxicity-efficacy studies
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+Handling covariates in the design of clinical trials
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+Convergence properties of sequential Bayesian \(D\)-optimal designs
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+Design of clinical trials involving multiple hypothesis tests with a common control
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+Implementing optimal allocation for sequential continuous responses with multiple treatments
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