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Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity

The most recent International Conference on Harmonisation E14 Q&A document states that a separate positive control would not be necessary provided sufficiently high exposures are achieved in the early‐phase studies. Realistically, a phase 1 study is unlikely to include a pharmacological positive...

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Autores principales: Ferber, Georg, Fernandes, Sara, Täubel, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763401/
https://www.ncbi.nlm.nih.gov/pubmed/28833240
http://dx.doi.org/10.1002/jcph.975
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author Ferber, Georg
Fernandes, Sara
Täubel, Jörg
author_facet Ferber, Georg
Fernandes, Sara
Täubel, Jörg
author_sort Ferber, Georg
collection PubMed
description The most recent International Conference on Harmonisation E14 Q&A document states that a separate positive control would not be necessary provided sufficiently high exposures are achieved in the early‐phase studies. Realistically, a phase 1 study is unlikely to include a pharmacological positive control, and in cases in which plasma levels of the drug exceeding therapeutic levels are not achieved, the lack of a positive control can constitute a limitation when excluding an effect of regulatory concern. It has been proposed to use the effect of a standardized meal on the estimate of the diurnal time course of QTc to show assay sensitivity. We conducted simulations by subsampling subjects from a 3 different studies and could show that the effect on food on QTc can be reliably prove assay sensitivity for sample sizes as low as 3 × 6 subjects with a power greater than 80%.
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spelling pubmed-57634012018-01-17 Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity Ferber, Georg Fernandes, Sara Täubel, Jörg J Clin Pharmacol Drug Development The most recent International Conference on Harmonisation E14 Q&A document states that a separate positive control would not be necessary provided sufficiently high exposures are achieved in the early‐phase studies. Realistically, a phase 1 study is unlikely to include a pharmacological positive control, and in cases in which plasma levels of the drug exceeding therapeutic levels are not achieved, the lack of a positive control can constitute a limitation when excluding an effect of regulatory concern. It has been proposed to use the effect of a standardized meal on the estimate of the diurnal time course of QTc to show assay sensitivity. We conducted simulations by subsampling subjects from a 3 different studies and could show that the effect on food on QTc can be reliably prove assay sensitivity for sample sizes as low as 3 × 6 subjects with a power greater than 80%. John Wiley and Sons Inc. 2017-08-17 2018-01 /pmc/articles/PMC5763401/ /pubmed/28833240 http://dx.doi.org/10.1002/jcph.975 Text en © 2017, The Authors. The Journal of Clinical Pharmacology published by Wiley Periodicals, Inc. on behalf of American College of Clinical Pharmacology This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Drug Development
Ferber, Georg
Fernandes, Sara
Täubel, Jörg
Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title_full Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title_fullStr Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title_full_unstemmed Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title_short Estimation of the Power of the Food Effect on QTc to Show Assay Sensitivity
title_sort estimation of the power of the food effect on qtc to show assay sensitivity
topic Drug Development
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763401/
https://www.ncbi.nlm.nih.gov/pubmed/28833240
http://dx.doi.org/10.1002/jcph.975
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