PO.ET07.01 · 实验与分子治疗
Quantitative Pharmacology and Translational Modeling
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1813 · PDF 用于ADC体内药代动力学分析的灵敏MSD-ECL平台 A sensitive MSD-ECL platform for in vivo pharmacokinetic profiling of ADCs Carla N. Castro, Jonas Hummel, Philipp Metzger, Cynthia Obodozie, Holger Weber
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1814 · PDF 用于抗体药物偶联物(ADC)全面表征的整合DMPK与生物分析平台 An integrated DMPK and bioanalytical platform for comprehensive characterization of antibody-drug conjugates (ADCs) Kefeng Gong, Xinhe Feng, Zhengyi Hua, Yanting Ma, Rui Wang, Xiaolong Tu, Luke Yu
- 1815 1815 SBE303的非临床表征:一种靶向nectin-4、搭载新型拓扑异构酶1抑制剂的抗体药物偶联物(ADC)显示出良好的安全边界 Nonclinical characterization of SBE303: A nectin-4 targeted antibody drug conjugate (ADC) with novel topoisomerase 1 inhibitor shows a favorable safety margin Ji Yeon Kim, Sungwoo Hyung, Hyun-Ji Choi, Songhyun Lim, Jae Hee Lee, Seokuee Kim, Donghyun Kim, So-Shin Ahn, Donghoon Shin
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1816 · PDF ACSL4介导的铁死亡及其在增强抗体药物偶联物疗效中的潜在作用 ACSL4 mediated ferroptosis and its potential role in enhancing the efficacy of antibody-drug conjugates Shigehiro Koganemaru, Hirobumi Fuchigami, Hiroshi Tsugawa, Hiroko Shinohara, Yasutoshi Kuboki, Toshimitsu Uenaka, Toshihiko Doi, Masahiro Yasunaga
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1818 · PDF 利用OBI-902克服耐药:新一代TROP2 ADC的临床前评价 Overcoming resistance with OBI-902: Preclinical evaluation of a next-generation TROP2 ADC Ren-Yu Hsu, Chi-Huan Lu, Chi-Sheng Shia, Jing-Rong Huang, Hsin-Shan Wu, Lu-Tzu Chen, Jhih-Jie Yang, Tzu-Min Yen, Jyy-Shiuan Tu, Yu-Hsuan Tsao, Ya-Chi Chen
- 1819 1819 OBI-904,一种基于聚糖的位点特异性Nectin-4靶向ADC,在非临床研究中表现出强效持久的抗肿瘤活性、改善的PK特征并克服EV耐药 OBI-904, a glycan-based site-specific Nectin-4-targeted ADC, demonstrates potent and durable antitumor activity with an improved PK profile and overcoming EV-resistance in non-clinical studies Chi-Huan Lu, Ren-Yu Hsu, Jing-Jie Ciou, Tzu-Min Yen, Jyy-Shiuan Tu, Yu-Hsuan Tsao, Jing-Rong Huang, Ya-Chi Chen
- 1820 1820 raludotatug deruxtecan(R-DXd)的药代动力学-肿瘤生长抑制建模,以支持铂耐药卵巢癌(PROC)的3期剂量选择 Pharmacokinetic-tumor growth inhibition modeling of raludotatug deruxtecan (R-DXd) to support phase 3 dose selection in platinum-resistant ovarian cancer (PROC) YoungJun Yoo, Kevin Koloskoff, Sandra Re, Izna Ali, Felipe K. Hurtado, Raouf El Cheikh
- 1821 1821 CS5006的临床前疗效与安全性,一种搭载拓扑异构酶1抑制剂载荷的新型整合素beta4靶向抗体药物偶联物 Preclinical efficacy and safety of CS5006, a novel integrin beta4-targeting antibody-drug conjugate with a topoisomerase 1 inhibitor payload Chuan Wang, Xinling Zhang, Ning Zhang, Yamin Wang, Yongwang Li, Mengyao Zhu, Xuelian Liu, Yaxin Chen, Yuxin Qian, Yongli Yang, Jingyu Sun, Fei Ma, Jianxin Yang
- 1822 1822 CS5008的临床前疗效与安全性,一种搭载拓扑异构酶1抑制剂载荷、用于小细胞肺癌和神经内分泌肿瘤的新型SSTR2×DLL3双特异性抗体药物偶联物(ADC) Preclinical efficacy and safety of CS5008, a novel SSTR2×DLL3 bispecific antibody-drug conjugate (ADC) with topoisomerase 1 inhibitor payload for small cell lung cancer and neuroendocrine tumors Chuan Wang, Yongwang Li, Ning Zhang, Yamin Wang, Xinling Zhang, Xuelian Liu, Yuxin Qian, Hui Dai, Xueqin Dai, Yaxin Chen, Zicong Zheng, Wenjing Xiang, Fei Ma, Jianxin Yang
- 1823 1823 CS5007的临床前疗效与安全性,一种搭载拓扑异构酶1抑制剂载荷的EGFR×HER3双靶向抗体药物偶联物 Preclinical efficacy and safety of CS5007, an EGFR×HER3 dual-targeting antibody-drug conjugate with a topoisomerase 1 inhibitor payload Chuan Wang, Yamin Wang, Ning Zhang, Xinling Zhang, Yongwang Li, Yuxin Qian, Yaxin Chen, Yongli Yang, Xuelian Liu, Mengyao Zhu, Hui Dai, Wenjing Xiang, Xueqin Dai, Fei Ma, Jianxin Yang
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1824 · PDF ORM-1153:一种新一代CD123靶向降解剂抗体偶联物(DAC) ORM-1153: A Next-Generation CD123-Targeting Degrader Antibody Conjugate (DAC) Adam T. Boutin, Dong-Ki Choi, YeonHee Yang, Jessica Alves, MinSoo Kim, Da-Yeong Kim, Khuloud Takrouri, Qinsi Zheng, Nadia Cherkassky, Anna Skaletskaya, Teresa Mako, VineetKumar Patil, Hangyeol Jeong, Olaf Christensen, Maysoun Shomali, Sang Hyun Lee, James Palacino
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1825 · PDF 用于指导TAK-280(一种双特异性抗体)剂量和给药方案选择的QSP建模 QSP modeling to inform dose and regimen selection for TAK-280: A bi-specific antibody Agnish Dey, Tao Long, Sabrina Collins, Dean Bottino, Jaydeep Srimani, John Gibbs
- 1826 1826 暴露-反应分析和定量系统药理学建模用于DLBCL患者中surovatamig的最佳剂量选择 Exposure-response analysis and quantitative systems pharmacology modeling for an optimal dose selection of surovatamig in patients with DLBCL Xu (Sue) Zhu, Damilola Olabode, Massimo Lai, Cesar Pichardo-Almarza, Meenu Pillai, Denise Brennan, David Sermer, Robin Lesley
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1827 · PDF PRC2抑制剂联合节拍化疗:弥漫性大B细胞淋巴瘤一种有前景的治疗策略 Combining PRC2 inhibitors with metronomic chemotherapy: A promising therapeutic strategy for diffuse large B-cell lymphoma Marta Banchi, Maryam Latarani, Paola Orlandi, Kayleigh Orchard, George Bryant, Francesco Crea, Guido Bocci
- 1828 1828 选择性强效EP300降解剂的临床前评估在血液系统恶性肿瘤中展示出强大的抗肿瘤活性和良好的耐受性 Preclinical evaluation of selective and potent EP300 degraders demonstrates robust antitumor activity and favorable tolerability in hematologic malignancies Meiyun Lin, Wesley Austin, Qianhe Zhuo, Rieko Arimoto, Karolina Mizeracka, Abira Ramakrishnan, Kevin Wilson, Elizabeth Wittenborn, Laura La Bonte, Steven Bellon
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1829 · PDF 通过p-选择素靶向递送EZH2 PROTAC治疗软脑膜中的乳腺癌脑转移 Treating breast cancer brain metastases in the leptomeninges through p-selectin targeted delivery of EZH2 PROTACs Raashed Raziuddin, Logan Hillger, Annie Ikemoto, Daniel Heller
- 1830 1830 SP09253,一种口服生物利用度高、高效力的RAS(ON)分子胶抑制剂,在KRAS突变肿瘤中展示出强大的抗肿瘤活性 SP09253, an orally bioavailable, highly potent RAS(ON) molecular glue inhibitor demonstrates robust anti-tumor activity in KRAS-mutant tumors Zherong Zhang, Xiaoyu Di, Qiming Sun
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1831 · PDF D3S-003(一种口服生物利用度高的双状态KRAS G12D抑制剂)的首次人体临床药代动力学预测 First-in-human clinical pharmacokinetic prediction of D3S-003, an orally bioavailable dual-state KRAS G12D inhibitor Shaonan Wang, Zhiqiang Zheng, Jing Zhang, Tienan Wang, Xin Xiong, Hui Wang, Zhijian Chen
- 1832 1832 钙调蛋白-PCAIs结合亲和力的计算机模拟与体外抗癌细胞活力:抗泛突变KRAS药物开发策略 In silico calmodulin-PCAIs binding affinities versus in vitro anticancer cell viability: Strategies for the development of anti-pan-mutant KRAS agents Jahnissi Frimpomah Odoom, Kweku Ofosu-Asante, Joshua Kofi Ablordeppey, Desmond Kwakye, Amarender Burra, Nazarius Lamango
- 1833 1833 多聚异戊二烯化半胱氨酰胺抑制剂抑制生长,诱导多种KRAS突变肺癌细胞的细胞骨架和转录组重塑 Polyisoprenylated cysteinyl amide inhibitors suppress growth, induce cytoskeletal and transcriptomic remodeling in multiple KRAS -mutated lung cancer cells Desmond Kwakye, Chase Lilly, Kweku Ofosu-Asante, Jahnissi Frimpomah Odoom, Joshua Kofi Ablordeppey, Bianca Dal Bó, KARLA GONZALEZ, Chunli Yan, Matthew A. Gladstone, Kyle R. Phillips, Benjamin J. Ryder, Yong Huang, Ite A. Offringa, Nazarius Lamango
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1834 · PDF 一种用于拟合调整AML或MDS患者阿扎胞苷剂量的数学模型 A mathematical model for fitting adjusting azacytidine in AML or SMD patients Quentin Gerbault, Loic Osanno, Joseph Ciccolini, Laure Farnault, Geoffroy Venton, Raphaelle Fanciullino
- 1835 1835 输液袋和生物基质中白消安稳定性的评价:在儿童常规治疗药物监测及适应性给药中的应用 Evaluation of busulfan stability in infusion bags and biological matrix: Application to routine therapeutic drug monitoring with adaptive dosing in children Marielle Jehanno, Jasmine Bettayeb, Guillaume Sicard, Arthur Sterin, Joseph Ciccolini
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1836 · PDF 转移性黑色素瘤患者中nivolumab暴露与疗效:一项真实世界研究 Nivolumab exposure and efficacy in metastatic melanoma patients: A real-world study Quentin Gerbault, Clara Boeri, Nausicaa Malissen, Caroline Gaudy, Joseph Ciccolini
- 1837 1837 靶向Hippo/YAP-TEAD可增强darovasertib在葡萄膜黑色素瘤中的抗肿瘤活性 Targeting Hippo/YAP-TEAD increases the antitumor activity of darovasertib in uveal melanoma Rodolfo Daniel Cervantes-Villagrana, Elena Sofia Cardenas Alcoser, Kuniaki Sato, Simone Lubrano, Tomohiko Ishikawa, Andrew E. Aplin, J. Silvio Gutkind
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1838 · PDF 三阴性乳腺癌的最优表观遗传学治疗 Optimal epigenetic therapies in triple-negative breast cancer Simone Bruno, Alexandra Indeglia, Sophia Lichterfeld, Karen M. Cichowski, Franziska Michor