The Clinical Development of Levodopa Inhalation Powder.

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Clinical Neuropharmacology Pub Date : 2023-03-01 DOI:10.1097/WNF.0000000000000540
Robert A Hauser, Peter A LeWitt, Cheryl H Waters, Donald G Grosset, Burkhard Blank
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引用次数: 2

Abstract

Abstract: Oral levodopa is the most effective treatment for Parkinson disease, but OFF periods emerge over time. Gastrointestinal dysfunction and food effects impact levodopa absorption, contributing to unpredictable control of OFF periods. Inhaled levodopa powder (Inbrija) is approved for on-demand treatment of OFF periods in patients receiving oral levodopa-dopa decarboxylase inhibitors. The 84-mg dose is administered via a breath-actuated inhaler. It provides pulmonary delivery of levodopa to the systemic circulation and is taken when a patient has an OFF period in between doses of regular oral levodopa medication. The pivotal SPAN-PD trial in patients experiencing OFF periods on oral dopaminergic therapy showed that levodopa inhalation powder 84 mg produced significant improvement in Unified Parkinson Disease Rating Scale Part III score, as measured 30 minutes postdose at week 12, and improvement was seen as early as 10 minutes. More patients in the levodopa inhalation powder group turned ON within 60 minutes of treatment and remained ON at 60 minutes than in the placebo group. Levodopa inhalation powder can also be used to treat early-morning OFF periods and, when used for up to 12 months, produced no clinically significant differences in pulmonary function compared with an untreated cohort. Levodopa inhalation powder 84 mg increased plasma levodopa concentration rapidly and with less variability than oral levodopa/carbidopa (25/100 mg). Most common adverse event associated with levodopa inhalation powder is cough, found in ~15% of patients in the SPAN-PD trial; otherwise, reported adverse events were consistent with those known to be associated with oral levodopa.

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左旋多巴吸入散的临床研究。
摘要:口服左旋多巴是帕金森病最有效的治疗方法,但随着时间的推移会出现OFF期。胃肠功能障碍和食物效应影响左旋多巴的吸收,导致OFF期的不可预测控制。吸入左旋多巴粉末(Inbrija)被批准用于口服左旋多巴-多巴脱羧酶抑制剂患者OFF期的按需治疗。84毫克的剂量是通过呼吸驱动吸入器给药的。它提供左旋多巴的肺部输送到体循环,当患者在常规口服左旋多巴药物之间有OFF期时服用。在口服多巴胺能治疗处于OFF期的患者中进行的关键SPAN-PD试验显示,在第12周给药后30分钟测量左旋多巴吸入粉末84 mg可显著改善统一帕金森病评定量表第III部分评分,并且早在10分钟就可以看到改善。与安慰剂组相比,左旋多巴吸入粉组在治疗60分钟内开启并在60分钟内保持开启的患者更多。左旋多巴吸入粉也可用于治疗清晨OFF期,并且在使用长达12个月时,与未治疗的队列相比,肺功能没有临床显着差异。左旋多巴吸入粉84 mg快速增加血浆左旋多巴浓度,且变异性小于口服左旋多巴/卡比多巴(25/100 mg)。与左旋多巴吸入性粉末相关的最常见不良事件是咳嗽,在SPAN-PD试验中约15%的患者中发现;除此之外,报告的不良事件与已知与口服左旋多巴相关的事件一致。
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来源期刊
Clinical Neuropharmacology
Clinical Neuropharmacology 医学-临床神经学
CiteScore
1.20
自引率
10.00%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Clinical Neuropharmacology is a peer-reviewed journal devoted to the pharmacology of the nervous system in its broadest sense. Coverage ranges from such basic aspects as mechanisms of action, structure-activity relationships, and drug metabolism and pharmacokinetics, to practical clinical problems such as drug interactions, drug toxicity, and therapy for specific syndromes and symptoms. The journal publishes original articles and brief reports, invited and submitted reviews, and letters to the editor. A regular feature is the Patient Management Series: in-depth case presentations with clinical questions and answers.
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