[促进利用人体样本提高制药公司临床反应可预测性的能力]。

Risa Okimoto, Takao Fujimura, Kayoko Mihara
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引用次数: 0

摘要

制药公司药物发现研究的一个问题是上市概率下降,需要通过进一步提高临床可预测性来提高概念验证(POC)的获得率。为此,我们需要加深对人类病理生理学的理解,并在新药研发阶段实现从 "动物 "到 "人类 "的思维转变,利用人类样本和数据提高新药研发的效率。特别是,为了提高利用人体样本/数据进行新药研发的效率,我们建立了人体样本利用支持能力,然后通过收集可提供各种人体样本的机构的信息和积累获取人体样本/数据的诀窍,支持获取适当的人体样本/数据,以满足各种新药研发需求。此外,我们还建立了一个一站式支持系统,用于调查人体样本/数据、与机构谈判和签约、获得伦理委员会批准、进口样本和办理通关手续。因此,我们的研究人员可以快速/轻松地获得高质量的人体样本/数据,满足他们的研究需求。通过建立这种能力,从药物发现的早期阶段开始,利用人体样本/数据实施靶点验证、药理学评估、BM 鉴定和患者分层等的研究项目数量不断增加,然后,利用人体样本/数据获得的证据为创造临床效果可能性高的候选药物做出了贡献。我们将介绍我们的活动,同时展示实际构建的支持流程。
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[A capability to promote the utilization of human samples for improving the ‍clinical response predictability in the pharmaceutical company].

An issue in drug discovery research at pharmaceutical companies is the decline in the probability of market launch, and there is a need to improve the proof-of-concept (POC) acquisition rate by further improving clinical predictability. For this purpose, we need to deepen our understanding of human pathophysiology, and to make efficient of drug discovery research by utilizing human samples and data due to the change in mindset from "animals" to "humans" at the drug discovery research stage. In particular, with the aim of improving the efficiency of drug discovery research by utilizing human samples/data, we have established a human sample utilization support capability, then we are supporting the acquisition of appropriate human samples/data to meet each drug research need with collecting information on organizations that can provide various human samples and accumulating know-how on obtaining human samples/data. In addition, we have built a one-stop support system for surveying human samples/data, negotiating, and contracting with the organizations, obtaining ethical committee approvals, importing samples, and dealing with customs clearance. As results, our researchers can obtain high-quality human samples/data to meet their research needs rapidly/easily. By establishing this capability, the number of the research projects that implement target validation, pharmacological evaluation, BM identification, and patient stratification, etc. using human samples/data from the early stage of drug discovery, has increased, and then, the evidence obtained by using human samples/data contribute to create drug candidates with high probability of clinical effect. We will introduce our activities while showing the support flow that was actually constructed.

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来源期刊
Folia Pharmacologica Japonica
Folia Pharmacologica Japonica Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
132
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