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Esketamine Nasal Spray in Major Depressive Disorder: A Meta-Analysis of Randomized Controlled Trials.

Zhibin Wang, Lili Jiang, Wenzhuang Ma, Xingyue Li, Qiushi Gao, Siyu Lian, Weiwei Yu

Clinical pharmacology and therapeutics June 1, 2025 DOI: 10.1002/cpt.3555 via PubMed

Summary

AI-generated from the abstract

A systematic review and meta-analysis of randomized controlled trials found that esketamine nasal spray, when used alongside an antidepressant, reduces depressive symptoms more than placebo in people with major depressive disorder. In patients without suicidal thoughts, symptoms improved by day 28; in those with suicidal thoughts, improvement was seen by day 2. Long-term relapse rates were 40% lower with esketamine than with placebo or quetiapine. The rate of suicidal ideation was similar between groups. The evidence was rated moderate to high certainty. Esketamine nasal spray appears to effectively control short- and long-term depressive symptoms with a manageable balance of benefits and risks.

Study at a glance

Characteristics Systematic review and meta-analysis Randomized Peer reviewed
Population Patients with major depressive disorder or treatment-resistant depression
Intervention Esketamine nasal spray
Keywords Mental health Depression treatment Medical breakthrough Antidepressants Psychiatric medicine
Citations 8
Key finding Esketamine nasal spray plus an antidepressant reduced depressive symptoms more than placebo in the short term and lowered long-term relapse rates by 40%.

Abstract

Despite being approved by the US FDA and the EU European Medicines Agency, the performance of esketamine nasal spray as an adjunctive therapy with an antidepressant in major depressive disorder is still controversial. Comprehensive retrieval in Embase, Pubmed, and Web of Science was conducted to identify randomized controlled trials comparing esketamine nasal spray versus control in major depressive disorder or treatment-resistant depression. The primary efficacy outcome was a reduction of the Montgomery-Asberg Depression Rating Scale, from baseline to Day 2 or Day 28 for patients with or without suicidal ideation, respectively. The long-term efficacy outcome was the relapse rate of patients who achieved stable remission. The certainty of evidence was assessed according to the Cochrane recommendation. Esketamine nasal spray was superior to placebo in reduction of Montgomery-Asberg Depression Rating Scale from baseline to Day 28 in patients without suicidal ideation (standardized mean difference: -0.24, 95% confidence interval: -0.38, -0.09, P = 0.001, I2 = 24%), and on Day 2 in patients with suicidal ideation (standardized mean difference: -0.30, 95% confidence interval: -0.47, -0.12, P = 0.0008, I2 = 0%). The long-term relapse rate was significantly lower in the esketamine nasal spray group than in the placebo/quetiapine group (risk ratio: RR: 0.60, 95% confidence interval: 0.45-0.80, I2 = 0%). The rate of suicidal ideation was similar between the two groups. The certainty of evidence was graded as "moderate" or "high" in the abovementioned results. Esketamine nasal spray in conjunction with an antidepressant effectively controls short-term and long-term depressive symptoms in major depressive disorder and treatment-resistant depression, with a manageable trade-off between efficacy and safety.

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