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July 10, 2024Journal of Biopharmaceutical Statistics0 citations

A constrained optimum adaptive design for dose finding in early phase clinical trials

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MAM. Iftakhar AlamBBBarbara BogackaDCD. Stephen Coad

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Abstract

Recently, interest has grown in the development of dose-finding methods that consider both toxicity and efficacy as endpoints. Along with responses on these, the incorporation of pharmacokinetic (PK) data can be beneficial in terms of patients' safety and can also increase the efficiency of the design for finding the best dose for the next phase. In this paper, the maximum concentration (

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Alam et al. (2024) studied this question.

synapsesocial.com/papers/68e60cdbb6db64358759fe19https://doi.org/10.1080/10543406.2024.2373452
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