AFQ056 Treatment of Levodopa-Induced Dyskinesias: Results of 2 Randomized Controlled Trials

被引:149
|
作者
Berg, Daniela [2 ,3 ]
Godau, Jana [2 ,3 ]
Trenkwalder, Claudia [4 ,5 ]
Eggert, Karla [6 ]
Csoti, Iiona [7 ]
Storch, Alexander [8 ]
Huber, Heiko [2 ,3 ]
Morelli-Canelo, Monica [4 ,5 ]
Stamelou, Maria [6 ]
Ries, Vincent [6 ]
Wolz, Martin [8 ]
Schneider, Christine [8 ]
Di Paolo, Therese [9 ,10 ]
Gasparini, Fabrizio [1 ]
Hariry, Sam [1 ]
Vandemeulebroecke, Marc [11 ]
Abi-Saab, Walid [1 ]
Cooke, Katy [12 ]
Johns, Donald [1 ]
Gomez-Mancilla, Baltazar [1 ]
机构
[1] Novartis Pharma AG, Neurosci Discovery, CH-4002 Basel, Switzerland
[2] Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany
[3] German Ctr Neurodegenerat Dis, Tubingen, Germany
[4] Univ Gottingen, D-3400 Gottingen, Germany
[5] Paracelsus Elena Klin, Kassel, Germany
[6] Univ Marburg, Marburg, Germany
[7] Gertrudis Klin, Biskirchen, Germany
[8] Tech Univ Dresden, Dept Neurol, D-8027 Dresden, Germany
[9] Univ Laval, Med Ctr, Mol Endocrinol & Genom Res Ctr, Quebec City, PQ, Canada
[10] Univ Laval, Fac Pharm, Quebec City, PQ, Canada
[11] Novartis Pharma AG, Translat Sci Biostat, CH-4002 Basel, Switzerland
[12] Alpha Plus Med Commun Ltd, High Wycombe, Bucks, England
关键词
parkinsonism; levodopa; glutamate antagonists; dyskinesias; METABOTROPIC GLUTAMATE RECEPTORS; DOPA-INDUCED DYSKINESIAS; PARKINSONS-DISEASE; MONKEYS; ANTAGONIST; MODEL; AMANTADINE; BLOCKADE;
D O I
10.1002/mds.23616
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study objectives were to assess the efficacy, safety, and tolerability of AFQ056 in Parkinson's disease patients with levodopa-induced dyskinesia. Two randomized, double-blind, placebo-controlled, parallel-group, in-patient studies for Parkinson's disease patients with moderate to severe levodopa-induced dyskinesia (study 1) and severe levodopa-induced dyskinesia (study 2) on stable dopaminergic therapy were performed. Patients received 25-150 mg AFQ056 or placebo twice daily for 16 days (both studies). Study 2 included a 4-day down-titration. Primary outcomes were the Lang-Fahn Activities of Daily Living Dyskinesia Scale (study 1), the modified Abnormal Involuntary Movement Scale (study 2), and the Unified Parkinson's Disease Rating Scale-part III both studies). Secondary outcomes included the Unified Parkinson's Disease Rating Scale-part IV items 32-33. The primary analysis was change from baseline to day 16 on all outcomes. Treatment differences were assessed. Fifteen patients were randomized to AFQ056 and 16 to placebo in study 1; 14 patients were randomized to each group in study 2. AFQ056-treated patients showed significant improvements in dyskinesias on day 16 versus placebo (eg, Lang-Fahn Activities of Daily Living Dyskinesia Scale, P = .021 [study 1]; modified Abnormal Involuntary Movement Scale, P = .032 [study 2]). No significant changes were seen from baseline on day 16 on the Unified Parkinson's Disease Rating Scale-part III in either study. Adverse events were reported in both studies, including dizziness. Serious adverse events (most commonly worsening of dyskinesias, apparently associated with stopping treatment) were reported by 4 AFQ056-treated patients in study 1, and 3 patients (2 AFQ056-treated patient and 1 in the placebo group) in study 2. AFQ056 showed a clinically relevant and significant antidyskinetic effect without changing the antiparkinsonian effects of dopaminergic therapy. (C) 2010 Movement Disorder Society
引用
收藏
页码:1243 / 1250
页数:8
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