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引用次数: 0
摘要
导言乳腺癌是全球最常见的癌症。约 70% 的乳腺癌表达雌激素受体 (ER),因此能够拮抗和降解 ER(SERDs)或与 ER 共价结合并拮抗 ER(SERCAs)的分子成为为患者提供更好治疗的前沿领域:本综述概述了2021年7月至2023年12月期间利用SciFinder发现的声称具有雌激素受体降解剂(SERD)和共价拮抗剂(SERCA)的专利申请。共评估了来自32个不同申请人的91项新专利申请,并将其分为酸性SERD、碱性SERD、SERCA和其他降解剂:氟维司群在治疗ER+乳腺癌方面的广泛应用继续刺激着对口服生物可利用型SERD和SERCA的研究。一些分子已进入临床开发阶段,尽管其中一些已经停产,但一批潜在的新疗法已产生了令人鼓舞的疗效和安全性数据。值得注意的是,首例口服 SERD 药物艾乐司群现已获得美国食品及药物管理局(FDA)和欧洲药物管理局(EMA)的批准,这进一步鼓励了此类靶向疗法的发展。
Selective estrogen receptor degraders (SERDs) and covalent antagonists (SERCAs): a patent review (July 2021-December 2023).
Introduction: Breast cancer is the most frequently diagnosed cancer worldwide. With around 70% of breast cancers expressing the estrogen receptor (ER), molecules capable of antagonizing and degrading ER (SERDs) or covalently binding to and antagonizing ER (SERCAs) are at the forefront of efforts to bring better treatments to patients.
Areas covered: This review summarizes patent applications that claim estrogen receptor degraders (SERDs) and covalent antagonists (SERCAs) identified using SciFinder between the period July 2021 to December 2023. A total of 91 new patent applications from 32 different applicants are evaluated with stratification into acidic SERDs, basic SERDs, SERCAs and miscellaneous degraders.
Expert opinion: The widespread adoption of fulvestrant in the treatment of ER+ breast cancer continues to stimulate research into orally bioavailable SERDs and SERCAs. A number of molecules have entered clinical development and, although some have been discontinued, a cohort of potential new treatments have generated encouraging efficacy and safety data. Notably, the first example of an oral SERD, elacestrant, has now been approved by the FDA and EMA, providing further encouragement for this class of targeted therapies.
期刊介绍:
Expert Opinion on Therapeutic Patents (ISSN 1354-3776 [print], 1744-7674 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on recent pharmaceutical patent claims, providing expert opinion the scope for future development, in the context of the scientific literature.
The Editors welcome:
Reviews covering recent patent claims on compounds or applications with therapeutic potential, including biotherapeutics and small-molecule agents with specific molecular targets; and patenting trends in a particular therapeutic area
Patent Evaluations examining the aims and chemical and biological claims of individual patents
Perspectives on issues relating to intellectual property
The audience consists of scientists, managers and decision-makers in the pharmaceutical industry and others closely involved in R&D
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