Opicapone as adjunct to levodopa in treated Parkinson's disease without motor complications: A randomized clinical trial

被引:0
|
作者
Ferreira, Joaquim J. [1 ,2 ]
Rascol, Olivier [3 ,4 ]
Stocchi, Fabrizio [5 ,6 ]
Antonini, Angelo [7 ]
Moreira, Joana [8 ]
Castilla-Fernandez, Guillermo [9 ]
Rocha, Jose-Francisco [8 ]
Holenz, Joerg [8 ]
Poewe, Werner [10 ]
Epsilon Study investigator
机构
[1] Univ Lisbon, Fac Med, iMM Inst Med Mol Joao Lobo Antunes, Lisbon, Portugal
[2] CNS, Campus Neurol, Torres Vedras, Portugal
[3] Univ Toulouse 3, Univ Hosp Toulouse, Clin Invest Ctr CIC1436, Ctr Excellence Neurodegenerat COEN NeuroToul,Dept, Toulouse, France
[4] Univ Toulouse 3, Univ Hosp Toulouse, NS Pk FCRIN Network, INSERM, Toulouse, France
[5] IRCCS San Raffaele Roma, Rome, Italy
[6] IRCCS San Raffaele, Inst Res & Med Care, Rome, Italy
[7] Univ Padua, Ctr Rare Neurol Dis ERN RND, Dept Neurosci, Parkinson & Movement Disorders Unit, Padua, Italy
[8] BIAL Portela & Ca SA, Coronado, Portugal
[9] BIAL R&D Investments, Coronado, Portugal
[10] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
关键词
clinical trial; COMT; levodopa; opicapone; Parkinson's disease; DOUBLE-BLIND; RATING-SCALE; LEVODOPA/CARBIDOPA; FLUCTUATIONS; ENTACAPONE; DIFFERENCE; INHIBITORS; EFFICACY; THERAPY; SAFETY;
D O I
10.1111/ene.16420
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Catechol-O-methyl transferase (COMT) inhibitors are routinely used to manage motor fluctuations in Parkinson's disease (PD). We assessed the effect of opicapone on motor symptom severity in levodopa-treated patients without motor complications. Methods This was a randomized, double-blind, 24-week, placebo-controlled study of opicapone 50 mg as adjunct to levodopa (NCT04978597). Levodopa-treated patients without motor complications were randomized to 24 weeks of double-blind treatment with adjunct opicapone 50 mg or matching placebo. The primary efficacy endpoint was the mean change from baseline to week 24 in Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III) total score. Results A total of 355 patients were randomized (opicapone 50 mg n = 177, placebo n = 178) and 322 (91%) completed the double-blind period. The adjusted mean [95% CI] change from baseline to week 24 in MDS-UPDRS-III subscore was -6.5 [-7.9, -5.2] in the opicapone group versus -4.3 [-5.7, 3.0] in the placebo group resulting in a significant difference of -2.2 [-3.9, -0.5] favoring opicapone (p = 0.010). There was no difference in the incidence of patients who developed motor complications (5.5% with opicapone vs. 9.8% with placebo) and the incidence of adverse events considered related to study medication was similar between groups (opicapone 10.2% vs. placebo 13.5%). Conclusions Treatment with once-daily adjunct opicapone was well tolerated, improved motor severity, and did not induce the development of motor complications. These results support the clinical usefulness of opicapone in the management of PD patients without motor complications.
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页数:10
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