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 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%.

[1]  P. Sager,et al.  Influence of Meals and Glycemic Changes on QT Interval Dynamics , 2017, Journal of clinical pharmacology.

[2]  P. Sager,et al.  Model‐Based Evaluation of Exenatide Effects on the QT Interval in Healthy Subjects Following Continuous IV Infusion , 2017, Journal of clinical pharmacology.

[3]  G. Ferber,et al.  Stability of the Effect of a Standardized Meal on QTc , 2017, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

[4]  Borje Darpo,et al.  Can Bias Evaluation Provide Protection Against False‐Negative Results in QT Studies Without a Positive Control Using Exposure‐Response Analysis? , 2017, Journal of clinical pharmacology.

[5]  A. Camm,et al.  Thorough QT study of the effect of intravenous amisulpride on QTc interval in Caucasian and Japanese healthy subjects , 2016, British journal of clinical pharmacology.

[6]  Y. Wang,et al.  Operational Characteristics of Linear Concentration‐QT Models for Assessing QTc Interval in the Thorough QT and Phase I Clinical Studies , 2016, Clinical pharmacology and therapeutics.

[7]  P. Maison-Blanche,et al.  Can an early phase clinical pharmacology study replace a thorough QT study? Experience with a novel H3-receptor antagonist/inverse agonist , 2016, European Journal of Clinical Pharmacology.

[8]  G. Ferber,et al.  The Power of Phase I Studies to Detect Clinical Relevant QTc Prolongation: A Resampling Simulation Study , 2015, BioMed research international.

[9]  P. Maison-Blanche,et al.  Establishing assay sensitivity in QT studies: experience with the use of moxifloxacin in an early phase clinical pharmacology study and comparison with its effect in a thorough QT study , 2015, European Journal of Clinical Pharmacology.

[10]  A. Camm,et al.  Single Doses up to 800 mg of E-52862 Do Not Prolong the QTc Interval – A Retrospective Validation by Pharmacokinetic-Pharmacodynamic Modelling of Electrocardiography Data Utilising the Effects of a Meal on QTc to Demonstrate ECG Assay Sensitivity , 2015, PloS one.

[11]  N. Stockbridge,et al.  Implications of the IQ-CSRC Prospective Study: Time to Revise ICH E14 , 2015, Drug Safety.

[12]  B. Darpo,et al.  Detection of QTc Effects in Small Studies—Implications for Replacing the Thorough QT Study , 2015, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

[13]  A. John Camm,et al.  Analyzing the relationship of QT interval and exposure to Nitazoxanide, a prospective candidate for influenza antiviral therapy—A formal TQT study , 2014, Journal of clinical pharmacology.

[14]  D. Bates,et al.  Fitting Linear Mixed-Effects Models Using lme4 , 2014, 1406.5823.

[15]  R Core Team,et al.  R: A language and environment for statistical computing. , 2014 .

[16]  A. Camm,et al.  Thorough QT study of the effect of oral moxifloxacin on QTc interval in the fed and fasted state in healthy Japanese and Caucasian subjects. , 2014, British journal of clinical pharmacology.

[17]  A. Camm,et al.  Shortening of the QT Interval After Food Can Be Used to Demonstrate Assay Sensitivity in Thorough QT Studies , 2012, Journal of clinical pharmacology.

[18]  M. Malik,et al.  Assessing electrocardiographic data quality and possible replacement of pharmacologic positive control in thorough QT/QTc studies by investigations of drug-free QTc stability. , 2011, Heart rhythm.

[19]  Borje Darpo,et al.  THEMED SECTION: QT SAFETY REVIEW The thorough QT/QTc study 4 years after the implementation of the ICH E14 guidance , 2010 .

[20]  L. S. Fridericia Die Systolendauer im Elektrokardiogramm bei normalen Menschen und bei Herzkranken , 2009 .

[21]  B. Odlind,et al.  Influence of food intake on electrocardiograms of healthy male volunteers , 1999, European Journal of Clinical Pharmacology.