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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

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Specialty Psychiatry
Date 2015 Nov 10
PMID 26549959
Citations 2
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Abstract

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.

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References
1.
Lecrubier Y . The burden of depression and anxiety in general medicine. J Clin Psychiatry. 2002; 62 Suppl 8:4-9; discussion 10-1. View

2.
Phillips M, Zhang J, Shi Q, Song Z, Ding Z, Pang S . Prevalence, treatment, and associated disability of mental disorders in four provinces in China during 2001-05: an epidemiological survey. Lancet. 2009; 373(9680):2041-53. DOI: 10.1016/S0140-6736(09)60660-7. View

3.
Kirwin J, Goren J . Duloxetine: a dual serotonin-norepinephrine reuptake inhibitor for treatment of major depressive disorder. Pharmacotherapy. 2005; 25(3):396-410. DOI: 10.1592/phco.25.3.396.61600. View

4.
Westanmo A, Gayken J, Haight R . Duloxetine: a balanced and selective norepinephrine- and serotonin-reuptake inhibitor. Am J Health Syst Pharm. 2005; 62(23):2481-90. DOI: 10.2146/ajhp050006. View

5.
Martinez J, Katon W, Greist J, Kroenke K, Thase M, Meyers A . A pragmatic 12-week, randomized trial of duloxetine versus generic selective serotonin-reuptake inhibitors in the treatment of adult outpatients in a moderate-to-severe depressive episode. Int Clin Psychopharmacol. 2011; 27(1):17-26. DOI: 10.1097/YIC.0b013e32834ce11b. View