University of South Florida, Tampa, FL, USA.
Parkinson's Disease and Movement Disorders Center of Boca Raton, Boca Raton, FL, USA.
Parkinsonism Relat Disord. 2019 Jul;64:175-180. doi: 10.1016/j.parkreldis.2019.03.026. Epub 2019 Mar 30.
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.
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.
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).
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.
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。
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。
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)。
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。