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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vormfelde, Stefan Viktor, Pezous, Nicole, Lefèvre, Gilbert, Kolly, Carine, Neumann, Ulf, Jordaan, Pierre, Ufer, Mike, Legangneux, Eric
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