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BRIVARACETAM: NEW COMPOUND APPROVED FOR THE TREATMENT OF EPILEPSY

机译:百乐精:批准用于治疗癫痫的新化合物

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Brivaracetam was approved in the E.U. and U.S. at the beginning of 2016 for the adjunctive treatment of focal epilepsies in patients over 16 years of age. This compound is a novel high-affinity synaptic vesicle glycoprotein 2A (SV2A) ligand, with a selectivity for this protein that is 10- to 30-fold higher than that shown by levetiracetam. Preclinical studies show that brivaracetam might have a stronger anticonvulsant effect and distributes in the brain more quickly, when compared to levetiracetam. The agent has linear and simple pharmacokinetics and a low interaction potential. Six double-blind placebo-controlled studies have assessed doses from 5 to 200 mg/day. Significant efficacy has been observed from doses of 50 mg/day, but there was not a clear dose-effect relationship. Short-term tolerability was excellent with all doses. Adverse events significantly associated with brivaracetam were dizziness, somnolence, fatigue and irritability. An excellent tolerability profile has been found after administration of a formulation for intravenous use.
机译:布里瓦西坦在欧盟获得批准。和美国在2016年初开始对16岁以上患者进行局灶性癫痫的辅助治疗。该化合物是一种新型的高亲和力突触囊泡糖蛋白2A(SV2A)配体,对该蛋白的选择性比左乙拉西坦所显示的高10至30倍。临床前研究表明,与左乙拉西坦相比,布瓦西坦可能具有更强的抗惊厥作用,并在脑中更快地分布。该剂具有线性和简单的药代动力学,并且相互作用潜力低。六项双盲安慰剂对照研究评估了5至200毫克/天的剂量。从50 mg /天的剂量观察到显着的疗效,但没有明确的剂量效应关系。所有剂量的短期耐受性都非常好。与溴氰西坦显着相关的不良事件是头晕,嗜睡,疲劳和易怒。在给予静脉内使用的制剂后发现了优异的耐受性。

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