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THALL, PETER F

One or more keywords matched the following items that are connected to THALL, PETER F

Item Type	Name
Concept	Computer Simulation
Academic Article	Accrual strategies for phase I trials with delayed patient outcome.
Academic Article	Practical model-based dose-finding in phase I clinical trials: methods based on toxicity.
Academic Article	Monitoring event times in early phase clinical trials: some practical issues.
Academic Article	Adaptive dose selection using efficacy-toxicity trade-offs: illustrations and practical considerations.
Academic Article	Simultaneously optimizing dose and schedule of a new cytotoxic agent.
Academic Article	Bayesian adaptive model selection for optimizing group sequential clinical trials.
Academic Article	Practical model-based dose finding in early-phase clinical trials: optimizing tissue plasminogen activator dose for treatment of ischemic stroke in children.
Academic Article	Evaluating multiple treatment courses in clinical trials.
Academic Article	Monitoring the rates of composite events with censored data in phase II clinical trials.
Academic Article	Continuous Bayesian adaptive randomization based on event times with covariates.
Academic Article	Bayesian designs to account for patient heterogeneity in phase II clinical trials.
Academic Article	Utility-based optimization of combination therapy using ordinal toxicity and efficacy in phase I/II trials.
Academic Article	Using joint utilities of the times to response and toxicity to adaptively optimize schedule-dose regimes.
Academic Article	Determining a maximum-tolerated schedule of a cytotoxic agent.
Academic Article	Statistical controversies in clinical research: scientific and ethical problems with adaptive randomization in comparative clinical trials.
Academic Article	Optimization of multi-stage dynamic treatment regimes utilizing accumulated data.
Academic Article	A simulation study of methods for selecting subgroup-specific doses in phase 1 trials.
Academic Article	A simulation study of outcome adaptive randomization in multi-arm clinical trials.
Academic Article	A utility-based design for randomized comparative trials with ordinal outcomes and prognostic subgroups.
Academic Article	Phase I-II clinical trial design: a state-of-the-art paradigm for dose finding.
Academic Article	A hybrid phase I-II/III clinical trial design allowing dose re-optimization in phase III.
Academic Article	Bayesian variable selection based on clinical relevance weights in small sample studies-Application to colon cancer.
Academic Article	An adaptive trial design to optimize dose-schedule regimes with delayed outcomes.
Academic Article	Bayesian cancer clinical trial designs with subgroup-specific decisions.
Academic Article	Comparing Bayesian early stopping boundaries for phase II clinical trials.
Academic Article	Comparison of Phase I-II designs with parametric or semi-parametric models using two different risk-benefit trade-off criteria.
Academic Article	Bayesian group sequential enrichment designs based on adaptive regression of response and survival time on baseline biomarkers.
Academic Article	Precision Bayesian phase I-II dose-finding based on utilities tailored to prognostic subgroups.
Academic Article	A Bayesian piecewise exponential phase II design for monitoring a time-to-event endpoint.
Academic Article	Bayesian treatment screening and selection using subgroup-specific utilities of response and toxicity.
Academic Article	Generalized phase I-II designs to increase long term therapeutic success rate.
Academic Article	BASIC: A Bayesian adaptive synthetic-control design for phase II clinical trials.
Academic Article	A generalized phase 1-2-3 design integrating dose optimization with confirmatory treatment comparison.

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Computer Simulation