Safety and effectiveness of vortioxetine in patients with major depressive disorder in a real-life clinical setting in India: results from an interventional, flexible-dose study.

IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL Current Medical Research and Opinion Pub Date : 2024-09-01 Epub Date: 2024-08-07 DOI:10.1080/03007995.2024.2382773
Michael Adair, Rohini Bose, Simon Nitschky Schmidt
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Abstract

Objective: Vortioxetine has demonstrated safety and efficacy in improving symptoms of major depressive disorder (MDD), including overall functioning in real-world settings. This is the first study in a real-life clinical setting in India to evaluate effectiveness and safety of vortioxetine in patients with MDD.

Methods: This interventional, open-label study consisted of a 12-week treatment period with flexible doses of vortioxetine (5-20 mg/day) in adult patients (aged 18-65 years) with a confirmed MDD diagnosis. Effectiveness outcomes included change from baseline to week 12 in Patient Health Questionnaire-9 (PHQ-9) and Clinical Global Impression-Severity (CGI-S) scores, along with CGI-Improvement (CGI-I) scores at week 12, using a mixed model for repeated measures. Adverse events (AEs) were recorded for safety outcome assessments.

Results: Of 395 patients who received vortioxetine, 42.3% were women mean age 38.9 years; 322 patients completed the study. Significant improvement in depressive symptoms was observed in change from baseline to week 12 least squares (LS) mean (SE) PHQ-9 total score (-9.36 [0.276]; p<.0001) and CGI-S score (-2.14 [0.065]; p<.0001). LS mean (SE) CGI-I score showed significant improvement at week 12 (1.93 [0.067]; p<.0001). Subgroup analysis across age, sex, disease severity, and body mass index showed significant improvements in depression symptoms and severity. A total of 35.4% (n = 140) of patients experienced treatment-emergent AEs (mostly mild-moderate); nausea and pruritus were the most frequent (6.6%, n = 26 each).

Conclusion: Safety and effectiveness of vortioxetine in improving symptoms of MDD over a 12-week period was demonstrated in a real-life clinical setting in India.

Clinical trial registration information: Open-label, flexible-dose study of vortioxetine in patients with major depressive disorder in India; Clinical Trials.gov ID: NCT04288895; https://www.clinicaltrials.gov/study/NCT04288895.

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在印度的真实临床环境中,伏替西汀对重度抑郁症患者的安全性和有效性:一项干预性灵活剂量研究的结果。
目的:伏替西汀在改善重度抑郁障碍(MDD)症状方面具有安全性和有效性,包括在实际环境中的整体功能。这是印度首次在真实的临床环境中评估伏替西汀对重度抑郁症患者的有效性和安全性:这项干预性开放标签研究包括为期 12 周的治疗,对确诊为 MDD 的成年患者(18-65 岁)使用灵活剂量的伏替西汀(5-20 毫克/天)。疗效结果包括患者健康问卷-9(PHQ-9)和临床总体印象-严重程度(CGI-S)评分从基线到第12周的变化,以及第12周时的CGI-改善(CGI-I)评分,采用的是重复测量混合模型。在安全性结果评估中记录了不良事件(AE):在接受伏替西汀治疗的 395 名患者中,42.3% 为女性,平均年龄为 38.9 岁;322 名患者完成了研究。从基线到第12周的最小二乘法(LS)平均值(SE)PHQ-9总分(-9.36 [0.276];ppn = 140)变化中观察到抑郁症状有显著改善:结论:在印度的实际临床环境中,伏替西汀在12周内改善MDD症状的安全性和有效性得到了证实:临床试验注册信息:印度重度抑郁症患者服用伏替西汀的开放标签、灵活剂量研究;Clinical Trials.gov ID:NCT04288895;https://www.clinicaltrials.gov/study/NCT04288895。
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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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