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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.
Afiliação
  • Vormfelde SV; Department of Translational Medicine, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Pezous N; Department of Translational Medicine, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Lefèvre G; Department of Translational Medicine, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Kolly C; Department of Preclinical Safety, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Neumann U; Department of Neuroscience, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Jordaan P; Cardiovascular Safety Expert - CMO and Patient Safety - Oncology, Novartis Pharma, Basel, Switzerland.
  • Ufer M; Department of Translational Medicine, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Legangneux E; Department of Translational Medicine, Novartis Institutes for BioMedical Research, Basel, Switzerland.
Clin Transl Sci ; 13(6): 1316-1326, 2020 11.
Article em En | MEDLINE | ID: mdl-32583957
ABSTRACT
Umibecestat, an orally active ß-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).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxazinas / Síndrome do QT Longo / Ácido Aspártico Endopeptidases / Eletrocardiografia / Secretases da Proteína Precursora do Amiloide Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxazinas / Síndrome do QT Longo / Ácido Aspártico Endopeptidases / Eletrocardiografia / Secretases da Proteína Precursora do Amiloide Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article