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Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France

INTRODUCTION: Esketamine nasal spray has been developed for patients with treatment resistant depression. OBJECTIVES: A cohort Temporary Authorization for Use (ATUc) allowed to collect for a 6-month period the first data in real life METHODS: On 02/08/2019 the French National Agency for Medicines an...

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Autores principales: Wattinne, E. Gaudre, Mekaoui, L., Rothärmel, M., Codet, M.A., Bouju, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480335/
http://dx.doi.org/10.1192/j.eurpsy.2021.1834
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author Wattinne, E. Gaudre
Mekaoui, L.
Rothärmel, M.
Codet, M.A.
Bouju, S.
author_facet Wattinne, E. Gaudre
Mekaoui, L.
Rothärmel, M.
Codet, M.A.
Bouju, S.
author_sort Wattinne, E. Gaudre
collection PubMed
description INTRODUCTION: Esketamine nasal spray has been developed for patients with treatment resistant depression. OBJECTIVES: A cohort Temporary Authorization for Use (ATUc) allowed to collect for a 6-month period the first data in real life METHODS: On 02/08/2019 the French National Agency for Medicines and Health Product Safety granted an early access program for Esketamine nasal spray framed by a specific protocol for patients without therapeutic alternatives. Each treatment request was approved based on inclusion and exclusion criteria. Clinical evolution, treatment management and safety were then spontaneously reported by psychiatrists. RESULTS: From 09/23/2019 to 03/25/2020, 66 patients were treated. The median age was 53 years and 41 (62.1%) were females. At treatment request, 52 patients (79%), presented a severe current depressive episode based on clinical judgment. The median duration of the disease was 12.2 years and the current episode was 2.6 years. Since the beginning of the current depressive episode, all patients (66) were prescribed ≥2 antidepressants (mean 4.2). Esketamine was initiated in a complete hospitalization setting in 27 patients (55.1%) and in day hospitalization in 22 patients (44.9%).Safety profile was consistent with the one described during clinical study. The most frequently adverse events reported (>10%) were dizziness, sedation, sleepiness, anxiety and dissociation. Most of them appeared after treatment administration and were transient. CONCLUSIONS: ATUc ended on 12/18/2019 after Marketing Authorization granted by European Medicines Agency. Data reported by French psychiatrists are the first collected in this specific population and provide descriptive information on patient characteristics, burden of disease; Esketamine management and practical use at hospital level DISCLOSURE: Data analysis performed by RCTs and poster conception coordinated by Medergy and funded by Janssen
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spelling pubmed-94803352022-09-29 Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France Wattinne, E. Gaudre Mekaoui, L. Rothärmel, M. Codet, M.A. Bouju, S. Eur Psychiatry Abstract INTRODUCTION: Esketamine nasal spray has been developed for patients with treatment resistant depression. OBJECTIVES: A cohort Temporary Authorization for Use (ATUc) allowed to collect for a 6-month period the first data in real life METHODS: On 02/08/2019 the French National Agency for Medicines and Health Product Safety granted an early access program for Esketamine nasal spray framed by a specific protocol for patients without therapeutic alternatives. Each treatment request was approved based on inclusion and exclusion criteria. Clinical evolution, treatment management and safety were then spontaneously reported by psychiatrists. RESULTS: From 09/23/2019 to 03/25/2020, 66 patients were treated. The median age was 53 years and 41 (62.1%) were females. At treatment request, 52 patients (79%), presented a severe current depressive episode based on clinical judgment. The median duration of the disease was 12.2 years and the current episode was 2.6 years. Since the beginning of the current depressive episode, all patients (66) were prescribed ≥2 antidepressants (mean 4.2). Esketamine was initiated in a complete hospitalization setting in 27 patients (55.1%) and in day hospitalization in 22 patients (44.9%).Safety profile was consistent with the one described during clinical study. The most frequently adverse events reported (>10%) were dizziness, sedation, sleepiness, anxiety and dissociation. Most of them appeared after treatment administration and were transient. CONCLUSIONS: ATUc ended on 12/18/2019 after Marketing Authorization granted by European Medicines Agency. Data reported by French psychiatrists are the first collected in this specific population and provide descriptive information on patient characteristics, burden of disease; Esketamine management and practical use at hospital level DISCLOSURE: Data analysis performed by RCTs and poster conception coordinated by Medergy and funded by Janssen Cambridge University Press 2021-08-13 /pmc/articles/PMC9480335/ http://dx.doi.org/10.1192/j.eurpsy.2021.1834 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Wattinne, E. Gaudre
Mekaoui, L.
Rothärmel, M.
Codet, M.A.
Bouju, S.
Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title_full Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title_fullStr Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title_full_unstemmed Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title_short Esketamine in patient with treatment resistant depression: Outcome of the temporary authorization for use programme in France
title_sort esketamine in patient with treatment resistant depression: outcome of the temporary authorization for use programme in france
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480335/
http://dx.doi.org/10.1192/j.eurpsy.2021.1834
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