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美国FDA已批准抗体-药物偶联物(ADC)OBI-999的IND

2019-09-04 Allan MedSci原创

OBI制药公司近日宣布,美国FDA已批准其抗体-药物偶联物(ADC)OBI-999的研究性新药申请(IND),将进行I/II期临床研究。OBI计划招募患有晚期实体瘤的患者,包括胰腺癌、胃癌、结直肠癌和食道癌。

OBI制药公司近日宣布,美国FDA已批准其抗体-药物偶联物(ADCOBI-999的研究性新药申请(IND),将进行I/II临床研究。OBI计划招募患有晚期实体瘤的患者,包括胰腺癌、癌、直肠癌和食道癌。OBI Pharma的首席医疗顾问,医学博士Tillman Pearce指出:这项临床试验旨在验证OBI-999的安全性和初步有效性。我们很高兴在德克萨斯大学MD安德森癌症中心进行这项临床试验,该中心是美国领先的肿瘤学研究机构之一

OBI Pharma董事长兼首席执行官Michael Chang博士补充说:“OBI-999是我们独特的抗Globo H肿瘤抗原的ADC。我们正努力开发新型抗Globo H的药物,以满足癌症患者的医疗需求


原始出处:

http://www.firstwordpharma.com/node/1663360#axzz5yVqufGke

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    2020-03-30 amy0550
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    2019-09-06 xiaogang319
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