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用于验证镇痛药物开发生物标志物的药理学探针。

Pharmacological Probes to Validate Biomarkers for Analgesic Drug Development.

机构信息

Mature Products Develoment, Grünenthal GmbH, 52099 Aachen, Germany.

Translational Science & Intelligence, Grünenthal GmbH, 52099 Aachen, Germany.

出版信息

Int J Mol Sci. 2022 Jul 27;23(15):8295. doi: 10.3390/ijms23158295.

DOI:10.3390/ijms23158295
PMID:35955432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9368481/
Abstract

There is an urgent need for analgesics with improved efficacy, especially in neuropathic and other chronic pain conditions. Unfortunately, in recent decades, many candidate analgesics have failed in clinical phase II or III trials despite promising preclinical results. Translational assessment tools to verify engagement of pharmacological targets and actions on compartments of the nociceptive system are missing in both rodents and humans. Through the Innovative Medicines Initiative of the European Union and EFPIA, a consortium of researchers from academia and the pharmaceutical industry was established to identify and validate a set of functional biomarkers to assess drug-induced effects on nociceptive processing at peripheral, spinal and supraspinal levels using electrophysiological and functional neuroimaging techniques. Here, we report the results of a systematic literature search for pharmacological probes that allow for validation of these biomarkers. Of 26 candidate substances, only 7 met the inclusion criteria: evidence for nociceptive system modulation, tolerability, availability in oral form for human use and absence of active metabolites. Based on pharmacokinetic characteristics, three were selected for a set of crossover studies in rodents and healthy humans. All currently available probes act on more than one compartment of the nociceptive system. Once validated, biomarkers of nociceptive signal processing, combined with a pharmacometric modelling, will enable a more rational approach to selecting dose ranges and verifying target engagement. Combined with advances in classification of chronic pain conditions, these biomarkers are expected to accelerate analgesic drug development.

摘要

特别在治疗神经痛和其他慢性疼痛疾病方面,我们急需更有效的止痛药物。但遗憾的是,尽管在临床前研究中取得了良好的效果,近几十年来,许多候选止痛药物在 II 期或 III 期临床试验中都失败了。在啮齿动物和人类中,缺乏用于验证药物作用于疼痛系统各部位的药理学靶点和作用的转化评估工具。通过欧盟创新药物倡议和 EFPIA,来自学术界和制药行业的研究人员建立了一个研究联盟,旨在使用电生理学和功能神经影像学技术,确定和验证一组用于评估外周、脊髓和脊髓上水平药物对伤害性加工影响的功能生物标志物。在这里,我们报告了一项用于验证这些生物标志物的药理学探针的系统文献检索结果。在 26 种候选物质中,只有 7 种符合纳入标准:有证据表明可调节疼痛系统、具有耐受性、可口服用于人体且无活性代谢物。根据药代动力学特征,选择了三种物质进行一组在啮齿动物和健康人类中的交叉研究。目前所有可用的探针都作用于疼痛系统的一个以上部位。这些生物标志物一旦经过验证,与药效计量建模相结合,将使我们能够更合理地选择剂量范围并验证靶点结合。结合慢性疼痛疾病分类的进展,这些生物标志物有望加速止痛药物的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/07bd023b874c/ijms-23-08295-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/c908de95bd69/ijms-23-08295-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/a9b33733815a/ijms-23-08295-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/616921be0eb1/ijms-23-08295-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/07bd023b874c/ijms-23-08295-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/c908de95bd69/ijms-23-08295-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/a9b33733815a/ijms-23-08295-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/616921be0eb1/ijms-23-08295-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11bf/9368481/07bd023b874c/ijms-23-08295-g004.jpg

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