Department of Neuroscience, Institute of Neurology, IRCCS San Raffaele Pisana, Roma, Italy.
Mov Disord. 2010 Sep 15;25(12):1881-7. doi: 10.1002/mds.23206.
Melevodopa hydrochloride plus carbidopa in effervescent tablets (M/C) is a readily soluble antiparkinsonian tablet formulation. A total of 221 patients with Parkinson's disease and motor fluctuations entered a randomized, double-blind, double-dummy, controlled parallel group study, which compared the effectiveness of oral M/C effervescent tablets with standard oral formulation levodopa/carbidopa tablets (L/C; Sinemet) in reducing total daily OFF time. The difference of total daily OFF time (intention-to-treat population) between the two groups was not statistically significant (P = 0.07): -39.4 minutes (95%CI: -67.08 to -11.73) in M/C group vs. +3.5 minutes (95%CI: -36.19 to +43.26) in the L/C group. In the intragroup analysis, M/C significantly reduced the baseline daily OFF, which remained unchanged in the L/C group. There were no unexpected adverse events in either treatment arms, and discontinuation rates due to adverse events did not differ between the two groups [M/C: 2 patients (1.3%); L/C: 1 patient (1.4%)]. This study failed to meet the primary endpoint (P = 0.07); however, there was a trend in favour of the M/C preparation, which deserves further attention.
盐酸美乐昔康与卡比多巴共晶(M/C)是一种易溶性抗帕金森病片剂配方。共有 221 名患有帕金森病和运动波动的患者参加了一项随机、双盲、双模拟、对照平行组研究,该研究比较了口服 M/C 泡腾片与标准口服左旋多巴/卡比多巴片(L/C;息宁)在减少每日总停药时间方面的有效性。两组之间的每日总停药时间差异(意向治疗人群)无统计学意义(P=0.07):M/C 组为-39.4 分钟(95%CI:-67.08 至-11.73),L/C 组为+3.5 分钟(95%CI:-36.19 至 43.26)。在组内分析中,M/C 显著减少了基线每日停药时间,而 L/C 组的停药时间没有变化。在两种治疗组中均未发生意外不良事件,且因不良事件而停药的发生率在两组之间无差异[M/C:2 例(1.3%);L/C:1 例(1.4%)]。本研究未达到主要终点(P=0.07);然而,M/C 制剂有改善的趋势,值得进一步关注。