Scholarlink

<p>Most of the about 30 clinically approved antiseizure medications (ASMs) have been discovered using animal seizure models. Thus, such models are commonly considered highly predictive of clinical antiseizure efficacy. However, this has recently been questioned by the apparent dichotomy in clinical antiseizure efficacy between the novel ASMs padsevonil and the alkyl-carbamate cenobamate, both of which were highly potent in a battery of acute and chronic rodent models. In this review, we analyze and compare the preclinical and clinical data for cenobamate and padsevonil, along with their proposed mechanisms of action, to identify differences between the two drugs that might have predicted the contrasting clinical outcome, as well as another alkyl-carbamate, carisbamate, which was highly effective in preclinical models but failed in clinical trials. While padsevonil was more potent than cenobamate and carisbamate in suppressing seizures in most acute and chronic animal models, an important difference was observed in the amygdala kindling model of focal epilepsy. Cenobamate suppressed both focal and secondary generalized convulsive seizures, whereas padsevonil was less effective against focal versus generalized seizures, and carisbamate was only partially effective&#xa0;in amygdala kindled rats. Padsevonil was developed in a target-based, rational drug design program that combined high affinity for synaptic vesicle glycoprotein 2 (SV2) with moderate affinity at the benzodiazepine binding site of the GABA<sub>A</sub> receptor, presuming that effects at these two targets would lead to a synergistic increase in antiseizure activity. However, it failed in human trials. In contrast, cenobamate, which was discovered by a chemocentric approach and phenotypic screening, exerted impressive clinical efficacy with a high rate of seizure freedom. The amygdala kindled rat was the only preclinical model that correctly predicted the successful and unsuccessful outcomes of clinical development of cenobamate, carisbamate, and padsevonil. Hopefully, the present analysis of three ASM discovery programs with largely diverging clinical outcomes will help to better understand the complexity and challenges of ASM development.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

The Complexity and Challenges of Developing Effective Epilepsy Therapies: Lessons to be Learned from Comparing Cenobamate, Carisbamate, and Padsevonil

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月31日

查看全文
  • Wolfgang Löscher,
  • H. Steve White,
  • Pavel Klein

摘要

Most of the about 30 clinically approved antiseizure medications (ASMs) have been discovered using animal seizure models. Thus, such models are commonly considered highly predictive of clinical antiseizure efficacy. However, this has recently been questioned by the apparent dichotomy in clinical antiseizure efficacy between the novel ASMs padsevonil and the alkyl-carbamate cenobamate, both of which were highly potent in a battery of acute and chronic rodent models. In this review, we analyze and compare the preclinical and clinical data for cenobamate and padsevonil, along with their proposed mechanisms of action, to identify differences between the two drugs that might have predicted the contrasting clinical outcome, as well as another alkyl-carbamate, carisbamate, which was highly effective in preclinical models but failed in clinical trials. While padsevonil was more potent than cenobamate and carisbamate in suppressing seizures in most acute and chronic animal models, an important difference was observed in the amygdala kindling model of focal epilepsy. Cenobamate suppressed both focal and secondary generalized convulsive seizures, whereas padsevonil was less effective against focal versus generalized seizures, and carisbamate was only partially effective in amygdala kindled rats. Padsevonil was developed in a target-based, rational drug design program that combined high affinity for synaptic vesicle glycoprotein 2 (SV2) with moderate affinity at the benzodiazepine binding site of the GABAA receptor, presuming that effects at these two targets would lead to a synergistic increase in antiseizure activity. However, it failed in human trials. In contrast, cenobamate, which was discovered by a chemocentric approach and phenotypic screening, exerted impressive clinical efficacy with a high rate of seizure freedom. The amygdala kindled rat was the only preclinical model that correctly predicted the successful and unsuccessful outcomes of clinical development of cenobamate, carisbamate, and padsevonil. Hopefully, the present analysis of three ASM discovery programs with largely diverging clinical outcomes will help to better understand the complexity and challenges of ASM development.