A randomized trial of inhaled levodopa (CVT-301) for motor fluctuations in Parkinson's disease

被引:84
作者
LeWitt, Peter A. [1 ,2 ]
Hauser, Robert A. [3 ]
Grosset, Donald G. [4 ]
Stocchi, Fabrizio [5 ]
Saint-Hilaire, Marie-Helene [6 ]
Ellenbogen, Aaron [7 ,8 ]
Leinonen, Mika [9 ]
Hampson, Neil B. [10 ]
DeFeo-Fraulini, Tia [11 ,13 ]
Freed, Martin I. [11 ,13 ]
Kieburtz, Karl D. [12 ]
机构
[1] Henry Ford Hosp, West Bloomfield, MI USA
[2] Wayne State Univ, Sch Med, West Bloomfield, MI USA
[3] Univ S Florida, Byrd Parkinson Dis & Movement Disorders Ctr, Tampa, FL USA
[4] Inst Neurol Sci, Glasgow, Lanark, Scotland
[5] IRCCS San Raffaele, Rome, Italy
[6] Boston Univ, Sch Med, Boston, MA 02118 USA
[7] Quest Res Inst, Farmington Hills, MI USA
[8] Michigan Inst Neurol Disorders, Farmington Hills, MI USA
[9] 4Pharma AB, Stockholm, Sweden
[10] Virginia Mason Med Ctr, Seattle, WA 98101 USA
[11] Acorda Therapeut, Chelsea, MA USA
[12] Clintrex LLC, Rye, NY USA
[13] Civitas Therapeut, Chelsea, MD USA
关键词
levodopa; Parkinson's disease; CVT-301; motor fluctuations; clinical trial; CLINICALLY IMPORTANT CHANGE; DOUBLE-BLIND; SUBCUTANEOUS APOMORPHINE; RATING-SCALE; OPEN-LABEL; PHARMACOKINETICS; SAFETY; THERAPY; LEVODOPA/CARBIDOPA; PHARMACODYNAMICS;
D O I
10.1002/mds.26611
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundAlthough levodopa is the most effective oral PD therapy, many patients experience motor fluctuations, including sudden loss of dose effect and delayed benefit. CVT-301 is a levodopa inhalation powder with the potential for rapid onset of action. The objective of this study was to evaluate CVT-301 self-administered by PD patients to relieve OFF episodes. MethodsPD patients with 2 hours per day of OFF time despite oral levodopa 4 times per day were randomized to CVT-301 or placebo for 4 weeks, to be used up to 3 times per day for OFF episodes. After 2 weeks, the study-drug dose was escalated from 35 to 50 mg. The primary end point was mean change in UPDRS Part III score from a predose OFF state to the average of postdose scores obtained at 10, 20, 30, and 60 minutes, as assessed in-clinic at the end of week 4. Home diaries were recorded. ResultsEighty-six patients used the study drug at an average frequency of 2.1 times per day for CVT-301 and for placebo. At 4 weeks, least-squares mean change in UPDRS Part III score favored CVT-301 by 7.0 points (P < 0.001). A treatment effect was evident at 10 minutes. At 4 weeks, least-squares mean OFF-time change from baseline favored CVT-301 by 0.9 hours per day (P = 0.045). The most frequently reported adverse events in the CVT-301 group were dizziness, cough, and nausea, each in 7% (3 of 43 patients). ConclusionsCVT-301 self-administered during OFF episodes provided rapid improvement of motor function, and daily OFF time was significantly reduced at the higher dose. CVT-301 was generally safe and well-tolerated. (c) 2016 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society
引用
收藏
页码:1356 / 1365
页数:10
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