晚期实体瘤双特异性抗pd -1/CTLA-4抗体。

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Pharmaceutical patent analyst Pub Date : 2020-09-01 Epub Date: 2020-09-22 DOI:10.4155/ppa-2020-0017
Martin Perez-Santos
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引用次数: 3

摘要

PD-1和CTLA-4是癌症免疫反应的检查点抑制剂,使它们成为开发治疗性抗体的靶分子。US2019161548专利描述了一种双特异性抗体,能够特异性结合PD-1和CTLA-4,诱导CD8+细胞的增殖和激活,以及在CD4+ T细胞中诱导共刺激物的表达。评估安全性、剂量限制性毒性和最大耐受/给药剂量的临床试验仍处于患者招募阶段,但科学和医学界非常感兴趣的是,第一个双特异性抗pd -1/CLTA-4抗体是否超出预期,并超过nivolumab和epilimumab联合治疗癌症的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bispecific anti-PD-1/CTLA-4 antibody for advanced solid tumors.

PD-1 and CTLA-4 are checkpoint inhibitors of the immune response in cancer, making them the target molecules for the development of therapeutic antibodies. US2019161548 patent describes a bispecific antibody capable of specifically binding to PD-1 and CTLA-4 that induced the proliferation and activation of CD8+ cells, as well as the expression of induclble co-stimulator in CD4+ T cells. Clinical trials to evaluate safety, dose-limiting toxicities and maximum tolerated/administered dose are still in the patient recruitment phase, but it will be of great interest to the scientific and medical community to know if the first bispecific anti-PD-1/CLTA-4 antibody, exceeds expectations and exceeds action of the combination of nivolumab and epilimumab in the treatment of cancer.

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来源期刊
Pharmaceutical patent analyst
Pharmaceutical patent analyst PHARMACOLOGY & PHARMACY-
CiteScore
1.80
自引率
0.00%
发文量
22
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