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Treatment of major depressive disorders with generic duloxetine and paroxetine: a multi-centered, double-blind, double-dummy, randomized controlled clinical trial
BACKGROUND: This study is a pre-registration trial of generic duloxetine that was approved by the China Food and Drug Administration (approval number: 2006L01603). AIMS: Compare the treatment efficacy and safety of generic duloxetine to that of paroxetine in patients with major depressive disorders...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shanghai Municipal Bureau of Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621288/ https://www.ncbi.nlm.nih.gov/pubmed/26549959 http://dx.doi.org/10.11919/j.issn.1002-0829.215064 |
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author | WANG, Zhiyang XU, Xiufeng TAN, Qingrong LI, Keqing MA, Cui XIE, Shiping GAO, Chengge WANG, Gang LI, Huafang |
author_facet | WANG, Zhiyang XU, Xiufeng TAN, Qingrong LI, Keqing MA, Cui XIE, Shiping GAO, Chengge WANG, Gang LI, Huafang |
author_sort | WANG, Zhiyang |
collection | PubMed |
description | BACKGROUND: This study is a pre-registration trial of generic duloxetine that was approved by the China Food and Drug Administration (approval number: 2006L01603). AIMS: Compare the treatment efficacy and safety of generic duloxetine to that of paroxetine in patients with major depressive disorders (MDD). METHODS: This was a double-dummy, double-blind, multicenter, positive drug (paroxetine), parallel randomized controlled clinical trial. The 299 patients with MDD recruited for the study were randomly assigned to use duloxetine (n=149; 40–60 mg/d) or paroxetine (n=150; 20 mg/d) for 8 weeks. The Hamilton Depression rating scale (HAMD-17) was administered at baseline and 1, 2, 4, 6, and 8 weeks after starting treatment. Remission was defined as a HAMD-17 score below 8 at the end of the trial, and treatment effectiveness was defined as a decrease in baseline HAMD-17 score of at least 50% by the end of the trial. Safety was assessed based on the reported prevalence and severity of side effects and changes in laboratory and electrocardiographic findings. Three patients in the duloxetine group dropped out before starting medication, so results were analyzed using a modified intention-to-treat (ITT) method with 146 in the experimental group and 150 in the control group. RESULTS: Both groups experienced 29 dropouts during the 8-week trial. HAMD-17 scores decreased significantly from baseline throughout the trial in both groups. Based on the ITT analysis, at the end of the trial there was no significant difference between the duloxetine group and the paroxetine group in effectiveness (67.1% v. 71.3%, X(2)=0.62 p=0.433), remission rate (41.1% v. 51.3%, X(2)=3.12, p=0.077), or in the incidence of side effects (56.8% v. 54.7%, X(2)=0.14, p=0.705). CONCLUSIONS: Generic duloxetine is as effective and safe as paroxetine in the acute treatment of patients with MDD who seek care at psychiatric outpatient departments in China. |
format | Online Article Text |
id | pubmed-4621288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Shanghai Municipal Bureau of Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-46212882015-11-06 Treatment of major depressive disorders with generic duloxetine and paroxetine: a multi-centered, double-blind, double-dummy, randomized controlled clinical trial WANG, Zhiyang XU, Xiufeng TAN, Qingrong LI, Keqing MA, Cui XIE, Shiping GAO, Chengge WANG, Gang LI, Huafang Shanghai Arch Psychiatry Original Research Article BACKGROUND: This study is a pre-registration trial of generic duloxetine that was approved by the China Food and Drug Administration (approval number: 2006L01603). AIMS: Compare the treatment efficacy and safety of generic duloxetine to that of paroxetine in patients with major depressive disorders (MDD). METHODS: This was a double-dummy, double-blind, multicenter, positive drug (paroxetine), parallel randomized controlled clinical trial. The 299 patients with MDD recruited for the study were randomly assigned to use duloxetine (n=149; 40–60 mg/d) or paroxetine (n=150; 20 mg/d) for 8 weeks. The Hamilton Depression rating scale (HAMD-17) was administered at baseline and 1, 2, 4, 6, and 8 weeks after starting treatment. Remission was defined as a HAMD-17 score below 8 at the end of the trial, and treatment effectiveness was defined as a decrease in baseline HAMD-17 score of at least 50% by the end of the trial. Safety was assessed based on the reported prevalence and severity of side effects and changes in laboratory and electrocardiographic findings. Three patients in the duloxetine group dropped out before starting medication, so results were analyzed using a modified intention-to-treat (ITT) method with 146 in the experimental group and 150 in the control group. RESULTS: Both groups experienced 29 dropouts during the 8-week trial. HAMD-17 scores decreased significantly from baseline throughout the trial in both groups. Based on the ITT analysis, at the end of the trial there was no significant difference between the duloxetine group and the paroxetine group in effectiveness (67.1% v. 71.3%, X(2)=0.62 p=0.433), remission rate (41.1% v. 51.3%, X(2)=3.12, p=0.077), or in the incidence of side effects (56.8% v. 54.7%, X(2)=0.14, p=0.705). CONCLUSIONS: Generic duloxetine is as effective and safe as paroxetine in the acute treatment of patients with MDD who seek care at psychiatric outpatient departments in China. Shanghai Municipal Bureau of Publishing 2015-08-25 /pmc/articles/PMC4621288/ /pubmed/26549959 http://dx.doi.org/10.11919/j.issn.1002-0829.215064 Text en Copyright © 2015 by Editorial Department of the Shanghai Archives of Psychiatry http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Original Research Article WANG, Zhiyang XU, Xiufeng TAN, Qingrong LI, Keqing MA, Cui XIE, Shiping GAO, Chengge WANG, Gang LI, Huafang Treatment of major depressive disorders with generic duloxetine and paroxetine: a multi-centered, double-blind, double-dummy, randomized controlled clinical trial |
title | Treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
title_full | Treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
title_fullStr | Treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
title_full_unstemmed | Treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
title_short | Treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
title_sort | treatment of major depressive disorders with generic
duloxetine and paroxetine: a multi-centered, double-blind,
double-dummy, randomized controlled clinical trial |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621288/ https://www.ncbi.nlm.nih.gov/pubmed/26549959 http://dx.doi.org/10.11919/j.issn.1002-0829.215064 |
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