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卡立普多,一种用于治疗癫痫的新型氨基甲酸盐。

Carisbamate, a new carbamate for the treatment of epilepsy.

作者信息

Kulig Katarzyna, Malawska Barbara

机构信息

Department of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688 Kraków, Poland.

出版信息

IDrugs. 2007 Oct;10(10):720-7.

Abstract

Carisbamate is a novel drug with neuromodulator activity that is currently under development for the treatment of epilepsy, diabetic neuropathy and neuralgia. The compound possessed a promising pharmacological profile in tests in vivo, and demonstrated broad anticonvulsant activity in preclinical studies, both elevating seizure threshold and preventing seizure spread. Carisbamate was also effective in protecting against spontaneous recurrent seizures in kainate-treated animals and in genetic models of epilepsy, and displayed antiepileptic and neuroprotective activity in the lithium-pilocarpine model of status epilepticus. In a phase I clinical trial, orally administered carisbamate demonstrated efficacy at high doses of 500 to 1000 mg. A phase II clinical trial confirmed that oral carisbamate was efficacious at a 300- to 1600-mg dose range. The preliminary evaluations of carisbamate in humans indicated complete absorption, extensive metabolism, and carbamate ester hydrolysis. The most frequently reported side effects associated with carisbamate are dizziness, headache, somnolence and nausea. In clinical trials, carisbamate did not display any significant interactions with commonly used antiepileptic drugs such as carbamazepine, valproate and lamotrigine. At the time of publication, a phase III clinical trial for carisbamate in the treatment of epilepsy was ongoing, as well as phase II trials in neuropathy and neuralgia. Data from preclinical brain injury studies with carisbamate and the analog RWJ-333369-A have also been reported. This drug profile will focus on the development of carisbamate in epilepsy.

摘要

卡立普多是一种具有神经调节活性的新型药物,目前正处于研发阶段,用于治疗癫痫、糖尿病性神经病变和神经痛。该化合物在体内试验中具有良好的药理学特性,并且在临床前研究中显示出广泛的抗惊厥活性,既能提高癫痫发作阈值,又能防止癫痫扩散。卡立普多在海藻酸处理的动物和癫痫遗传模型中对自发性反复癫痫发作也有预防作用,并且在癫痫持续状态的锂-匹鲁卡品模型中表现出抗癫痫和神经保护活性。在一项I期临床试验中,口服卡立普多在500至1000毫克的高剂量下显示出疗效。一项II期临床试验证实,口服卡立普多在300至1600毫克的剂量范围内有效。卡立普多在人体中的初步评估表明其吸收完全、代谢广泛,且存在氨基甲酸酯水解。与卡立普多相关的最常见副作用是头晕、头痛、嗜睡和恶心。在临床试验中,卡立普多与常用抗癫痫药物如卡马西平、丙戊酸盐和拉莫三嗪之间未显示出任何显著相互作用。在本文发表时,卡立普多治疗癫痫的III期临床试验正在进行中,同时针对神经病变和神经痛的II期试验也在进行。关于卡立普多及其类似物RWJ - 333369 - A在临床前脑损伤研究中的数据也已被报道。本药物简介将聚焦于卡立普多在癫痫治疗方面的研发进展。

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