Cargando…
A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat
Umibecestat, an orally active β‐secretase inhibitor, reduces the production of amyloid beta‐peptide that accumulates in the brain of patients with Alzheimer’s disease. The echocardiogram effects of umibecestat, on QTcF (Fridericia‐corrected QT), on PR and QRS and heart rate (HR), were estimated by c...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719381/ https://www.ncbi.nlm.nih.gov/pubmed/32583957 http://dx.doi.org/10.1111/cts.12832 |
_version_ | 1783619667362840576 |
---|---|
author | Vormfelde, Stefan Viktor Pezous, Nicole Lefèvre, Gilbert Kolly, Carine Neumann, Ulf Jordaan, Pierre Ufer, Mike Legangneux, Eric |
author_facet | Vormfelde, Stefan Viktor Pezous, Nicole Lefèvre, Gilbert Kolly, Carine Neumann, Ulf Jordaan, Pierre Ufer, Mike Legangneux, Eric |
author_sort | Vormfelde, Stefan Viktor |
collection | PubMed |
description | Umibecestat, an orally active β‐secretase inhibitor, reduces the production of amyloid beta‐peptide that accumulates in the brain of patients with Alzheimer’s disease. The echocardiogram effects of umibecestat, on QTcF (Fridericia‐corrected QT), on PR and QRS and heart rate (HR), were estimated by concentration‐effect modeling. Three phase I/II studies with durations up to 3 months, with 372 healthy subjects over a wide age range, including both sexes and 2 ethnicities, were pooled, providing a large data set with good statistical power. No clinically relevant effect on QTcF, PR interval, QRS duration, or HR were observed up to supratherapeutic doses. The upper bound of 90% confidence intervals of the ∆QTcF was below the 10 ms threshold of regulatory concern for all concentrations measured. Prespecified sensitivity analysis confirmed the results in both sexes, in those over and below 60 years, and in Japanese subjects. All conclusions were endorsed by the US Food and Drug Administration (FDA). |
format | Online Article Text |
id | pubmed-7719381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77193812020-12-11 A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat Vormfelde, Stefan Viktor Pezous, Nicole Lefèvre, Gilbert Kolly, Carine Neumann, Ulf Jordaan, Pierre Ufer, Mike Legangneux, Eric Clin Transl Sci Research Umibecestat, an orally active β‐secretase inhibitor, reduces the production of amyloid beta‐peptide that accumulates in the brain of patients with Alzheimer’s disease. The echocardiogram effects of umibecestat, on QTcF (Fridericia‐corrected QT), on PR and QRS and heart rate (HR), were estimated by concentration‐effect modeling. Three phase I/II studies with durations up to 3 months, with 372 healthy subjects over a wide age range, including both sexes and 2 ethnicities, were pooled, providing a large data set with good statistical power. No clinically relevant effect on QTcF, PR interval, QRS duration, or HR were observed up to supratherapeutic doses. The upper bound of 90% confidence intervals of the ∆QTcF was below the 10 ms threshold of regulatory concern for all concentrations measured. Prespecified sensitivity analysis confirmed the results in both sexes, in those over and below 60 years, and in Japanese subjects. All conclusions were endorsed by the US Food and Drug Administration (FDA). John Wiley and Sons Inc. 2020-07-23 2020-11 /pmc/articles/PMC7719381/ /pubmed/32583957 http://dx.doi.org/10.1111/cts.12832 Text en © 2020 Novartis Institutes for BioMedical Research. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the 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 | Research Vormfelde, Stefan Viktor Pezous, Nicole Lefèvre, Gilbert Kolly, Carine Neumann, Ulf Jordaan, Pierre Ufer, Mike Legangneux, Eric A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title | A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title_full | A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title_fullStr | A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title_full_unstemmed | A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title_short | A Pooled Analysis of Three Randomized Phase I/IIa Clinical Trials Confirms Absence of a Clinically Relevant Effect on the QTc Interval by Umibecestat |
title_sort | pooled analysis of three randomized phase i/iia clinical trials confirms absence of a clinically relevant effect on the qtc interval by umibecestat |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719381/ https://www.ncbi.nlm.nih.gov/pubmed/32583957 http://dx.doi.org/10.1111/cts.12832 |
work_keys_str_mv | AT vormfeldestefanviktor apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT pezousnicole apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT lefevregilbert apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT kollycarine apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT neumannulf apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT jordaanpierre apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT ufermike apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT legangneuxeric apooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT vormfeldestefanviktor pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT pezousnicole pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT lefevregilbert pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT kollycarine pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT neumannulf pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT jordaanpierre pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT ufermike pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat AT legangneuxeric pooledanalysisofthreerandomizedphaseiiiaclinicaltrialsconfirmsabsenceofaclinicallyrelevanteffectontheqtcintervalbyumibecestat |