Efficacy and Safety of Valbenazine in Elderly and Nonelderly Japanese Patients With Tardive Dyskinesia: A Post Hoc Analysis of the J-KINECT Study.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Yumi Watanabe, Yutaka Susuta, Mieko Nagano, Hideaki Masui, Nobuhisa Kanahara
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引用次数: 0

Abstract

Purpose: The efficacy and safety of valbenazine, a selective vesicular monoamine transporter 2 inhibitor, has been confirmed for treatment of tardive dyskinesia (TD) in patients aged ≥65 years in non-Asian clinical trials; however, data are lacking in elderly Asian patients. This post hoc analysis of J-KINECT aimed to evaluate the efficacy and safety of valbenazine in elderly Japanese patients with TD.

Methods: J-KINECT was a randomized, double-blind, placebo-controlled study with a 6-week double-blind, placebo-controlled period; 42-week double-blind, valbenazine extension period; and 4-week posttreatment observation period. Outcomes were summarized by age (≥65 years [elderly] and <65 [nonelderly]) and treatment group.

Results: The safety analysis set included 100 and 153 patients aged ≥65 and <65 years, respectively (intention-to-treat set: 98 and 151 patients, respectively). In the elderly group, the difference versus placebo in least-squares mean change from baseline in the Abnormal Involuntary Movement Scale total score at week 6 was -3.1 (95% confidence interval: -4.5, -1.7) and -5.5 (-7.0, -3.9) with valbenazine 40 and 80 mg, respectively; in the nonelderly group, respective differences were -1.5 (-2.6, -0.4) and -2.5 (-3.6, -1.3). Both age groups showed improvement in Clinical Global Impression of Change-Tardive Dyskinesia scores with valbenazine. The incidence of treatment-emergent adverse events (TEAEs) leading to treatment discontinuation was higher in the elderly versus nonelderly group. There was no trend toward higher incidences of TEAEs or related TEAEs in the elderly group.

Conclusions: The findings suggest that valbenazine may be used effectively and safely as a treatment for TD, even in elderly patients.

戊苯那嗪对日本老年和非老年迟发性运动障碍患者的疗效和安全性:J-KINECT 研究的事后分析》。
目的:在非亚洲的临床试验中,选择性囊泡单胺转运体2抑制剂戊苯那嗪治疗年龄≥65岁的迟发性运动障碍(TD)的有效性和安全性已得到证实;然而,在亚洲老年患者中缺乏相关数据。本研究对 J-KINECT 进行了事后分析,旨在评估缬苯嗪对日本老年 TD 患者的疗效和安全性:J-KINECT是一项随机、双盲、安慰剂对照研究,为期6周的双盲、安慰剂对照期;42周的双盲、缬苯嗪延长期;以及4周的治疗后观察期。研究结果按年龄(≥65 岁[老年人]和结果)进行了汇总:安全性分析集包括 100 名和 153 名年龄≥65 岁的患者和结论:研究结果表明,即使是老年患者,也可以有效、安全地使用戊苯那嗪治疗 TD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
3.40%
发文量
231
审稿时长
4-8 weeks
期刊介绍: Journal of Clinical Psychopharmacology, a leading publication in psychopharmacology, offers a wide range of articles reporting on clinical trials and studies, side effects, drug interactions, overdose management, pharmacogenetics, pharmacokinetics, and psychiatric effects of non-psychiatric drugs. The journal keeps clinician-scientists and trainees up-to-date on the latest clinical developments in psychopharmacologic agents, presenting the extensive coverage needed to keep up with every development in this fast-growing field.
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