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口服左旋多巴(CVT-301)治疗帕金森病清晨关期。

Orally inhaled levodopa (CVT-301) for early morning OFF periods in Parkinson's disease.

机构信息

University of South Florida, Tampa, FL, USA.

Parkinson's Disease and Movement Disorders Center of Boca Raton, Boca Raton, FL, USA.

出版信息

Parkinsonism Relat Disord. 2019 Jul;64:175-180. doi: 10.1016/j.parkreldis.2019.03.026. Epub 2019 Mar 30.

Abstract

BACKGROUND

CVT-301 (Inbrija) is a self-administered orally inhaled levodopa approved for the intermittent treatment of OFF episodes in patients with Parkinson's disease (PD) treated with carbidopa/levodopa. Prior studies only evaluated CVT-301 after the first ON of the day.

OBJECTIVE AND METHODS

The objective of this study was to evaluate the safety and tolerability of CVT-301 for early morning OFF. Using a randomized, double-blind, 2-way crossover design, eligible patients in the morning OFF state (having not received PD medication overnight) received a single dose of CVT-301 84 mg or placebo on 2 dosing days, immediately after their first morning oral carbidopa/levodopa dose. Safety assessments included treatment-emergent adverse events, vital signs, and patient- and examiner-reported dyskinesia. An exploratory efficacy assessment was examiner-rated time-to-ON with carbidopa/levodopa + CVT-301 vs carbidopa/levodopa + placebo.

RESULTS

Of the 36 patients (mean age 62.9 years) who enrolled and completed the study, 9 (25.0%) reported treatment-emergent adverse events following CVT-301 administration; 4 (11.1%) reported treatment-emergent adverse events following placebo. The most common adverse event was cough (4 [11.1%] for CVT-301 vs 1 [2.8%] for placebo), which was typically mild and transient. Incidence of asymptomatic orthostatic hypotension (CVT-301, 6; placebo, 7) and examiner-rated dyskinesia were similar for both (36-39% mild, 3-6% moderate, and 0% severe). Median time-to-ON was 25.0 min following carbidopa/levodopa + CVT-301 and 35.5 min following carbidopa/levodopa + placebo (P = 0.26). At 30 min, more patients had turned ON following carbidopa/levodopa + CVT-301 administration (66.7%), compared with carbidopa/levodopa + placebo (44.5%) (P = 0.040).

CONCLUSION

Single doses of CVT-301 84 mg administered with oral carbidopa/levodopa for early morning OFF symptoms were well-tolerated, with no notable safety concerns.

摘要

背景

CVT-301(Inbrija)是一种自行口服吸入的左旋多巴,适用于接受卡比多巴/左旋多巴治疗的帕金森病患者的间歇性治疗。先前的研究仅评估了 CVT-301 在一天中的第一次 ON 后。

目的和方法

本研究的目的是评估 CVT-301 治疗清晨 OFF 的安全性和耐受性。使用随机、双盲、2 向交叉设计,在早晨 OFF 状态下(整夜未接受 PD 药物治疗)的合格患者在 2 个给药日中,在接受第一剂早晨口服卡比多巴/左旋多巴后立即接受 CVT-301 84mg 或安慰剂单次剂量。安全性评估包括治疗后出现的不良事件、生命体征以及患者和检查者报告的运动障碍。探索性疗效评估是检查者评估 CVT-301 与卡比多巴/左旋多巴+安慰剂与卡比多巴/左旋多巴+CVT-301 相比的 ON 时间。

结果

36 名(平均年龄 62.9 岁)入组并完成研究的患者中,9 名(25.0%)在接受 CVT-301 治疗后报告了治疗后出现的不良事件;4 名(11.1%)在接受安慰剂后报告了治疗后出现的不良事件。最常见的不良事件是咳嗽(CVT-301 为 4[11.1%],安慰剂为 1[2.8%]),通常是轻度和短暂的。无症状直立性低血压(CVT-301 为 6;安慰剂为 7)和检查者评估的运动障碍的发生率在两者之间相似(36-39%为轻度,3-6%为中度,0%为重度)。卡比多巴/左旋多巴+CVT-301 后中位 ON 时间为 25.0 分钟,卡比多巴/左旋多巴+安慰剂后为 35.5 分钟(P=0.26)。在 30 分钟时,与卡比多巴/左旋多巴+安慰剂相比,更多的患者在接受卡比多巴/左旋多巴+CVT-301 治疗后 ON(66.7%)(P=0.040)。

结论

在清晨 OFF 症状时给予口服卡比多巴/左旋多巴,单次给予 CVT-301 84mg 耐受性良好,无明显安全性问题。

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