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Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers
BACKGROUND AND OBJECTIVE: Tucatinib is a selective tyrosine kinase inhibitor of the human epidermal growth factor receptor 2 (HER2) approved to treat metastatic HER2-positive breast and colorectal cancers. The International Council for Harmonisation of Technical Requirements for Human Use (ICH) E14...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676329/ https://www.ncbi.nlm.nih.gov/pubmed/37751113 http://dx.doi.org/10.1007/s40268-023-00440-8 |
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author | Topletz-Erickson, Ariel R. Mayor, JoAl G. Liu, Hsu-Tai Abdulrasool, Layth I. Endres, Christopher J. |
author_facet | Topletz-Erickson, Ariel R. Mayor, JoAl G. Liu, Hsu-Tai Abdulrasool, Layth I. Endres, Christopher J. |
author_sort | Topletz-Erickson, Ariel R. |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Tucatinib is a selective tyrosine kinase inhibitor of the human epidermal growth factor receptor 2 (HER2) approved to treat metastatic HER2-positive breast and colorectal cancers. The International Council for Harmonisation of Technical Requirements for Human Use (ICH) E14 guideline mandates that new drugs are assessed for potential effects on cardiac repolarization through electrocardiogram (ECG) evaluation in a QT/corrected QT (TQT) study. METHODS: We evaluated the effect of tucatinib on cardiac repolarization in healthy volunteers in a phase I, randomized, partially double-blind, placebo-and positive-controlled three-period crossover study. The primary endpoint was the placebo-corrected change from baseline in QT interval values, corrected for heart rate using Fridericia’s method (ΔΔQTcF). RESULTS: After achieving steady-state tucatinib exposures with 300 mg twice daily, the observed ΔΔQTcF ranged from −2.9 msec at 2 hours post-dose to 0 msec at 4 hours post-dose. The upper bound of the 90% confidence interval (CI) was below 5 ms at all post-dose timepoints. Assay sensitivity was confirmed as the lower bound of the 90% CI and was >5 ms following moxifloxacin dosing. As the mean ΔΔQTcF of tucatinib was predicted to be − 1.80 ms (90% CI − 3.90, 0.30) at clinically relevant tucatinib concentrations (511 ng/mL), an effect of tucatinib on QTcF exceeding 10 ms was excluded within observed ranges of tucatinib (up to ~1000 ng/mL). Tucatinib had no clinically relevant effect on heart rate or cardiac conduction. The safety profile of tucatinib was manageable after multiple doses. CONCLUSION: Tucatinib had no clinically relevant effects on studied ECG parameters. This study constitutes a clearly negative TQT study per ICH E14 guidance. CLINICAL TRIAL REGISTRATION: This trial (NCT03777761) was registered on 17 December 2018. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40268-023-00440-8. |
format | Online Article Text |
id | pubmed-10676329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-106763292023-09-26 Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers Topletz-Erickson, Ariel R. Mayor, JoAl G. Liu, Hsu-Tai Abdulrasool, Layth I. Endres, Christopher J. Drugs R D Original Research Article BACKGROUND AND OBJECTIVE: Tucatinib is a selective tyrosine kinase inhibitor of the human epidermal growth factor receptor 2 (HER2) approved to treat metastatic HER2-positive breast and colorectal cancers. The International Council for Harmonisation of Technical Requirements for Human Use (ICH) E14 guideline mandates that new drugs are assessed for potential effects on cardiac repolarization through electrocardiogram (ECG) evaluation in a QT/corrected QT (TQT) study. METHODS: We evaluated the effect of tucatinib on cardiac repolarization in healthy volunteers in a phase I, randomized, partially double-blind, placebo-and positive-controlled three-period crossover study. The primary endpoint was the placebo-corrected change from baseline in QT interval values, corrected for heart rate using Fridericia’s method (ΔΔQTcF). RESULTS: After achieving steady-state tucatinib exposures with 300 mg twice daily, the observed ΔΔQTcF ranged from −2.9 msec at 2 hours post-dose to 0 msec at 4 hours post-dose. The upper bound of the 90% confidence interval (CI) was below 5 ms at all post-dose timepoints. Assay sensitivity was confirmed as the lower bound of the 90% CI and was >5 ms following moxifloxacin dosing. As the mean ΔΔQTcF of tucatinib was predicted to be − 1.80 ms (90% CI − 3.90, 0.30) at clinically relevant tucatinib concentrations (511 ng/mL), an effect of tucatinib on QTcF exceeding 10 ms was excluded within observed ranges of tucatinib (up to ~1000 ng/mL). Tucatinib had no clinically relevant effect on heart rate or cardiac conduction. The safety profile of tucatinib was manageable after multiple doses. CONCLUSION: Tucatinib had no clinically relevant effects on studied ECG parameters. This study constitutes a clearly negative TQT study per ICH E14 guidance. CLINICAL TRIAL REGISTRATION: This trial (NCT03777761) was registered on 17 December 2018. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40268-023-00440-8. Springer International Publishing 2023-09-26 2023-12 /pmc/articles/PMC10676329/ /pubmed/37751113 http://dx.doi.org/10.1007/s40268-023-00440-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Article Topletz-Erickson, Ariel R. Mayor, JoAl G. Liu, Hsu-Tai Abdulrasool, Layth I. Endres, Christopher J. Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title | Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title_full | Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title_fullStr | Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title_full_unstemmed | Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title_short | Effect of Tucatinib on Cardiac Repolarization in Healthy Volunteers |
title_sort | effect of tucatinib on cardiac repolarization in healthy volunteers |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676329/ https://www.ncbi.nlm.nih.gov/pubmed/37751113 http://dx.doi.org/10.1007/s40268-023-00440-8 |
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