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Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study
PURPOSE: The primary objective of this study was to assess long-term safety with sublingual asenapine 2.5 or 5 mg twice daily (BID) in patients with schizophrenia. PATIENTS AND METHODS: Actively treated patients on asenapine 2.5 mg BID, asenapine 5 mg BID, or olanzapine 15 mg once daily (QD) who com...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546824/ https://www.ncbi.nlm.nih.gov/pubmed/28814871 http://dx.doi.org/10.2147/NDT.S130211 |
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author | Durgam, Suresh Landbloom, Ronald P Mackle, Mary Wu, Xiao Mathews, Maju Nasrallah, Henry A |
author_facet | Durgam, Suresh Landbloom, Ronald P Mackle, Mary Wu, Xiao Mathews, Maju Nasrallah, Henry A |
author_sort | Durgam, Suresh |
collection | PubMed |
description | PURPOSE: The primary objective of this study was to assess long-term safety with sublingual asenapine 2.5 or 5 mg twice daily (BID) in patients with schizophrenia. PATIENTS AND METHODS: Actively treated patients on asenapine 2.5 mg BID, asenapine 5 mg BID, or olanzapine 15 mg once daily (QD) who completed a 6-week randomized, double-blind, placebo- and olanzapine-controlled study continued lead-in treatment in this 26-week, multicenter, double-blind, double-dummy, olanzapine-controlled Phase IIIB extension study; placebo patients were assigned to asenapine 2.5 mg BID treatment. Safety analyses were based on the all treated set (patients who received one or more doses of extension trial medication); change from baseline analyses used the acute study baseline. Treatment-emergent adverse events (TEAEs) and changes in laboratory parameters were monitored; weight change for asenapine versus olanzapine was the key secondary objective. Descriptive statistics were used; weight change was analyzed using a mixed-model repeated-measure approach. RESULTS: Of the 120 patients in the all-treated set, 60% completed treatment (asenapine 2.5 mg BID 66.1% overall, asenapine 5 mg BID 52.4%, olanzapine 15 mg QD 56.3%). The incidence of TEAEs was higher for placebo patients from the lead-in study who switched to asenapine 2.5 mg BID for extension treatment (71.0%) versus patients continuing asenapine 2.5 mg BID (38.7%), asenapine 5 mg BID (38.1%), or olanzapine 15 mg QD (25.0%). The most common TEAE (≥5% in every group) was worsening of schizophrenia. Least squares mean change in body weight from the acute study baseline to week 26 was +0.6 kg for overall asenapine 2.5 mg BID, +0.8 kg for asenapine 5 mg BID, and +1.2 kg for olanzapine 15 mg QD. There were no clinically relevant changes in metabolic parameters; values were generally similar across treatment groups. CONCLUSION: Asenapine 2.5 mg BID and 5 mg BID were generally well tolerated in long-term treatment. Weight gain was less for overall asenapine 2.5 mg BID and 5 mg BID than for olanzapine 15 mg QD. |
format | Online Article Text |
id | pubmed-5546824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55468242017-08-16 Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study Durgam, Suresh Landbloom, Ronald P Mackle, Mary Wu, Xiao Mathews, Maju Nasrallah, Henry A Neuropsychiatr Dis Treat Original Research PURPOSE: The primary objective of this study was to assess long-term safety with sublingual asenapine 2.5 or 5 mg twice daily (BID) in patients with schizophrenia. PATIENTS AND METHODS: Actively treated patients on asenapine 2.5 mg BID, asenapine 5 mg BID, or olanzapine 15 mg once daily (QD) who completed a 6-week randomized, double-blind, placebo- and olanzapine-controlled study continued lead-in treatment in this 26-week, multicenter, double-blind, double-dummy, olanzapine-controlled Phase IIIB extension study; placebo patients were assigned to asenapine 2.5 mg BID treatment. Safety analyses were based on the all treated set (patients who received one or more doses of extension trial medication); change from baseline analyses used the acute study baseline. Treatment-emergent adverse events (TEAEs) and changes in laboratory parameters were monitored; weight change for asenapine versus olanzapine was the key secondary objective. Descriptive statistics were used; weight change was analyzed using a mixed-model repeated-measure approach. RESULTS: Of the 120 patients in the all-treated set, 60% completed treatment (asenapine 2.5 mg BID 66.1% overall, asenapine 5 mg BID 52.4%, olanzapine 15 mg QD 56.3%). The incidence of TEAEs was higher for placebo patients from the lead-in study who switched to asenapine 2.5 mg BID for extension treatment (71.0%) versus patients continuing asenapine 2.5 mg BID (38.7%), asenapine 5 mg BID (38.1%), or olanzapine 15 mg QD (25.0%). The most common TEAE (≥5% in every group) was worsening of schizophrenia. Least squares mean change in body weight from the acute study baseline to week 26 was +0.6 kg for overall asenapine 2.5 mg BID, +0.8 kg for asenapine 5 mg BID, and +1.2 kg for olanzapine 15 mg QD. There were no clinically relevant changes in metabolic parameters; values were generally similar across treatment groups. CONCLUSION: Asenapine 2.5 mg BID and 5 mg BID were generally well tolerated in long-term treatment. Weight gain was less for overall asenapine 2.5 mg BID and 5 mg BID than for olanzapine 15 mg QD. Dove Medical Press 2017-07-31 /pmc/articles/PMC5546824/ /pubmed/28814871 http://dx.doi.org/10.2147/NDT.S130211 Text en © 2017 Durgam et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Durgam, Suresh Landbloom, Ronald P Mackle, Mary Wu, Xiao Mathews, Maju Nasrallah, Henry A Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title | Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title_full | Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title_fullStr | Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title_full_unstemmed | Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title_short | Exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
title_sort | exploring the long-term safety of asenapine in adults with schizophrenia in a double-blind, fixed-dose, extension study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546824/ https://www.ncbi.nlm.nih.gov/pubmed/28814871 http://dx.doi.org/10.2147/NDT.S130211 |
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