01 吉利德科学公司宣布,美国FDA已授予Trodelvy突破性疗法认定,用于治疗接受铂类化疗后疾病进展的广泛期小细胞肺癌 (ES-SCLC)成人患者。 04 目前,Trodelvy已在超过50个国家和地区获批,用于治疗经治转移性三阴性乳腺癌 ...
Gilead Sciences GILD announced that its first-in-class Trop-2-directed antibody-drug conjugate, Trodelvy (sacituzumab ...
Gilead Sciences, Inc. has announced that Trodelvy (sacituzumab govitecan-hziy) has received Breakthrough Therapy Designation ...
在其他发展方面,吉利德科学公司的调查性HIV预防药物Lenacapavir在关键的三期试验中显示HIV感染减少了96%。Deutsche ...
在其他近期新闻中,生物技术公司吉利德科学公司的药物Trodelvy获得了美国食品和药物管理局的突破性疗法认定,用于治疗特定形式的肺癌。这一认定是基于Phase 2 ...
The US Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to Trodelvy (sacituzumab ...
11月27日,科伦博泰的TROP2-ADC药物芦康沙妥珠单抗获国家药品监督管理局批准上市,用于治疗既往至少接受过2种系统治疗的不可切除的局部晚期或转移性三阴性乳腺癌(TNBC)成人患者。成为国内上市的首个国产TROP2-ADC药物,也是中国首个获得完 ...
Gilead (GILD) announced that the FDA has granted Breakthrough Therapy Designation to Trodelvy for the treatment of adult patients with ...
(RTTNews) - Gilead Sciences, Inc. (GILD) Tuesday said that the U.S. Food and Drug Administration or FDA has granted Breakthrough Therapy Designation to Trodelvy for the treatment of adults with ...
智通财经APP获悉,天风证券发布研究报告称,首次覆盖科伦博泰生物-B(06990),予以“增持”评级,预计公司2024-2026年营业收入分别为12.17亿元、16.54亿元和24.76亿元;归母净利润分别为-7.20亿元、-6.06亿元、-4.15 ...
SKB264是国产进度第一,全球进度前三的TROP2ADC,同处于第一梯队还有吉列德的Trodelvy和第一三共的DS-1062。默沙东围绕公司核心产品SKB264(MK-2870 ...