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Novel concentration‐QTc models for early clinical studies with parallel placebo controls: A simulation study
Author(s) -
Orihashi Yasushi,
Kumagai Yuji,
Shiosakai Kazuhito
Publication year - 2020
Publication title -
pharmaceutical statistics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.421
H-Index - 38
eISSN - 1539-1612
pISSN - 1539-1604
DOI - 10.1002/pst.2083
Subject(s) - qt interval , dosing , medicine , covariance , placebo , pharmacology , statistics , mathematics , alternative medicine , pathology
The QTc interval of the electrocardiogram is a pharmacodynamic biomarker for drug‐induced cardiac toxicity. The ICH E14 guideline Questions and Answers offer a solution for evaluating a concentration‐QTc relationship in early clinical studies as an alternative to conducting a thorough QT/QTc study. We focused on covariance structures of QTc intervals on the baseline day and dosing day (two‐day covariance structure,) and proposed a two‐day QTc model to analyze a concentration‐QTc relationship for placebo‐controlled parallel phase 1 single ascending dose studies. The proposed two‐day QTc model is based on a constrained longitudinal data analysis model and a mixed effects model, thus allowing various variance components to capture the two‐day covariance structure. We also propose a one‐day QTc model for the situation where no baseline day or only a pre‐dose baseline is available and models for multiple ascending dose studies where concentration and QTc intervals are available over multiple days. A simulation study shows that the proposed models control the false negative rate for positive drugs and have both higher accuracy and power for negative drugs than existing models in a variety of settings for the two‐day covariance structure. The proposed models will promote early and accurate evaluation of the cardiac safety of new drugs.