4.7 Article

A multicenter, randomized, double-blind, duloxetine-controlled, non-inferiority trial of desvenlafaxine succinate extended-release in patients with major depressive disorder

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 329, 期 -, 页码 72-80

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ELSEVIER
DOI: 10.1016/j.jad.2023.02.067

关键词

Desvenlafaxine; Duloxetine; Major depressive disorder; Non-inferiority; 17-item Hamilton Depression Rating Scale

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This study compared the efficacy and safety of Desvenlafaxine and duloxetine in treating patients with MDD. The results showed that Desvenlafaxine was non-inferior to duloxetine in efficacy and had a lower incidence of adverse events.
Background: Desvenlafaxine and duloxetine are selective serotonin and norepinephrine reuptake inhibitors. Their efficacy has not been directly compared using statistical hypotheses. This study evaluated the non-inferiority of desvenlafaxine extended-release (XL) to duloxetine in patients with major depressive disorder (MDD).Methods: In this study, 420 adult patients with moderate-to-severe MDD were enrolled and randomly assigned (1:1) to receive 50 mg (once daily [QD]) of desvenlafaxine XL (n = 212) or 60 mg QD of duloxetine (n = 208). The primary endpoint was evaluated using a non-inferiority comparison based on the change from baseline to 8 weeks in the 17-item Hamilton Depression Rating Scale (HAM-D17) total score. Secondary endpoints and safety were evaluated.Results: Least-squares mean change in HAM-D17 total score from baseline to 8 weeks was-15.3 (95% confidence interval [CI]:-17.73,-12.89) in the desvenlafaxine XL group and -15.9 (95% CI,-18.44,-13.39) in the duloxetine group. The least-squares mean difference was 0.6 (95% CI:-0.48, 1.69), and the upper boundary of 95% CI was less than the non-inferiority margin (2.2). No significant between-treatment differences were found in most secondary efficacy endpoints. The incidence of the most common treatment-emergent adverse events (TEAEs) was lower for desvenlafaxine XL than for duloxetine for nausea (27.2% versus 48.8%) and dizziness (18.0% versus 28.8%).Limitations: A short-term non-inferiority study without a placebo arm.Conclusions: This study demonstrated that desvenlafaxine XL 50 mg QD was non-inferior to duloxetine 60 mg QD in efficacy in patients with MDD. Desvenlafaxine had a lower incidence of TEAEs than duloxetine did.

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