The FDA has granted breakthrough therapy designation Trodelvy for adults with extensive-stage small cell lung cancer who ...
ES-SCLC is a form of lung cancer accounting for one in eight lung cancer cases in the UK. It is an aggressive disease that progresses rapidly, with a significant negative impact on the quality of ...
Gilead Sciences GILD announced that its first-in-class Trop-2-directed antibody-drug conjugate, Trodelvy (sacituzumab ...
A Phase 2 study showed encouraging results with Trodelvy as a second-line treatment for extensive-stage small cell lung ...
Gilead Sciences, Inc. has announced that Trodelvy (sacituzumab govitecan-hziy) has received Breakthrough Therapy Designation ...
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 ...
GSK’s GSK’227 has gained Priority Medicines (PRIME) designation from the EMA for the treatment of relapsed ES-SCLC.
GSK’s B7-H3-targeted antibody-drug conjugate, GSK’227 gets EMA PRIME designation in relapsed extensive-stage small-cell lung cancer: London Saturday, December 21, 2024, 17:30 ...
Gilead Sciences announced that the FDA has granted Breakthrough Therapy Designation to breast cancer drug Trodelvy (sacituzumab govitecan-hziy) for the treatment of adult patients with extensive-stage ...
2024年12月18日,苏州宜联生物医药有限公司(以下简称“宜联生物医药”),一家处于临床阶段的生物科技公司,宣布其自主研发的抗体偶联药物YL201获得美国食品和药物管理局(FDA)授予的孤儿药资格认定(Orphan-drug Designation),用于治疗小细胞肺癌(SCLC)。YL201是一款基于宜联自主创新的TMALIN®技术平台的靶向B7H3的ADC药物。 目前,YL201项目正在全球 ...
In September 2024, Gilead announced a strategic partnership with Genesis Therapeutics, focusing on AI to discover and develop ...
眼下,据复宏汉霖执行董事、首席执行官朱俊博士形容,复宏汉霖进入了出海全球化2.0时代的“深水区”,接下来,在与各国家和地区的全球化共舞中,通过本地化能力的建设,致力于成为生物医药届出海的“领航者”。在中国的生物制药公司中,已经成立14年的复宏汉霖(2 ...