摘要:INCB86550的发现:一种有效的口服生物可利用的小分子PDL1抑制剂,用于治疗癌症

Liangxing Wu
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引用次数: 1

摘要

用治疗性抗体阻断PD-(L)1免疫检查点轴已被证明是多种癌症组织学的有效治疗方式。口服生物可利用的PD-1/PD-L1相互作用的小分子抑制剂被高度期待为单克隆抗体的有希望的替代或补充治疗。本报告将详细介绍我们的发现演变,导致发现一流的小分子PDL1抑制剂INCB89550,目前正在临床试验中用于治疗癌症。该报告还将详细介绍我们对PD-(L)1轴的新型小分子拮抗剂的表征,这些拮抗剂通过诱导PD- l1蛋白的二聚化和随后的内化,有效地从细胞膜上消耗配体,并阻止PD-1在T细胞上的激活。引用格式:吴良兴。INCB86550的发现:一种有效的口服小分子PDL1抑制剂,用于治疗癌症[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr ND01。
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Abstract ND01: Discovery of INCB86550: A potent, orally bioavailable small molecule inhibitor of PDL1 for the treatment of cancer
Blocking the PD-(L)1 immune checkpoint axis with therapeutic antibodies has proven to be an effective treatment modality for multiple cancer histologies. Orally bioavailable small-molecule inhibitors of the PD-1/PD-L1 interaction have been highly anticipated as a promising alternative or complementary therapeutic to the monoclonal antibodies. This presentation will detail our discovery evolution that led to the discovery of a first-in-class small molecule PDL1 inhibitor INCB89550 which is currently in clinical trials for the treatment of cancer. The presentation will also detail our characterization of novel small molecule antagonists of the PD-(L)1 axis that function by inducing dimerization and subsequent internalization of the PD-L1 protein, effectively depleting the ligand from the cell membrane and preventing PD-1 activation on T cells. Citation Format: Liangxing Wu. Discovery of INCB86550: A potent, orally bioavailable small molecule inhibitor of PDL1 for the treatment of cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr ND01.
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