Nomoto Masahiro, Nagai Masahiro, Nishikawa Noriko, Ando Rina, Kagamiishi Yoshifumi, Yano Koji, Saito Shigeto, Takeda Atsushi
Department of Neurology and Clinical Pharmacology, Clinical Research Trial Center, Phase-I Unit, Ehime University Graduate School of Medicine, Tohon, Ehime, Japan.
Translational Medicine Center, Ono Pharmaceutical Co., Ltd, Osaka, Japan.
eNeurologicalSci. 2018 Sep 17;13:8-13. doi: 10.1016/j.ensci.2018.09.003. eCollection 2018 Dec.
We conducted a phase I study investigating the efficacy, safety, and tolerability of ONO-2160, a newly developed levodopa pro-drug, and carbidopa compared with levodopa and carbidopa to stabilize levodopa plasma concentration fluctuations in Japanese patients with Parkinson's disease. In an open-label two-period design, patients ( = 12) with Parkinson's disease received levodopa and carbidopa for 3 days before 7 days of treatment with ONO-2160 and carbidopa. Patients were primarily evaluated using the Unified Parkinson's Disease Rating Scale Part III, a Parkinson's disease symptom diary, and analysis of adverse events. Pharmacokinetic analysis of plasma levodopa concentration was also performed. ONO-2160 and carbidopa therapy stabilized effective plasma levodopa concentration. No adverse events with safety concerns were observed. The combination of ONO-2160 and carbidopa produced a prolonged and stable plasma levodopa concentration with a reduction in Unified Parkinson's Disease Rating Scale Part III total scores. The combination was well tolerated, with no safety concerns, when administered to Japanese patients with Parkinson's disease.
我们开展了一项I期研究,调查新开发的左旋多巴前体药物ONO-2160与卡比多巴联合使用时,相较于左旋多巴与卡比多巴联合使用,在稳定日本帕金森病患者左旋多巴血药浓度波动方面的疗效、安全性和耐受性。在一项开放标签的两阶段设计中,12例帕金森病患者在接受7天的ONO-2160与卡比多巴治疗前,先接受3天的左旋多巴与卡比多巴治疗。主要通过统一帕金森病评定量表第三部分、帕金森病症状日记以及不良事件分析对患者进行评估。同时还进行了血浆左旋多巴浓度的药代动力学分析。ONO-2160与卡比多巴联合治疗可稳定有效的血浆左旋多巴浓度。未观察到有安全问题的不良事件。ONO-2160与卡比多巴联合使用可使血浆左旋多巴浓度延长且稳定,同时统一帕金森病评定量表第三部分的总分降低。该联合用药在用于日本帕金森病患者时耐受性良好,无安全问题。