In Silico Biosciences, PA, USA.
Future Med Chem. 2014;6(16):1757-69. doi: 10.4155/fmc.14.97.
Clinical development in brain diseases has one of the lowest success rates in the pharmaceutical industry, and many promising rationally designed single-target R&D projects fail in expensive Phase III trials. By contrast, successful older CNS drugs do have a rich pharmacology. This article will provide arguments suggesting that highly selective single-target drugs are not sufficiently powerful to restore complex neuronal circuit homeostasis. A rationally designed multitarget project can be derisked by dialing in an additional symptomatic treatment effect on top of a disease modification target. Alternatively, we expand upon a hypothetical workflow example using a humanized computer-based quantitative systems pharmacology platform. The hope is that incorporating rationally multipharmacology drug discovery could potentially lead to more impactful polypharmacy drugs.
脑疾病的临床开发是制药行业成功率最低的领域之一,许多有前途的合理设计的单靶标研发项目在昂贵的 III 期试验中失败。相比之下,成功的旧中枢神经系统药物确实具有丰富的药理学。本文将提供论据,表明高度选择性的单靶标药物不足以强大到恢复复杂的神经元回路内稳态。通过在疾病修饰靶点之上增加额外的对症治疗效果,可以降低合理设计的多靶标项目的风险。或者,我们可以在使用基于计算机的人类定量系统药理学平台的假设工作流程示例的基础上进行扩展。希望通过合理的多药理学药物发现,有可能开发出更有影响力的多药联合疗法药物。