搜索优化
English
搜索
Copilot
图片
视频
地图
资讯
购物
更多
航班
旅游
酒店
房地产
笔记本
Top stories
Sports
U.S.
Local
World
Science
Technology
Entertainment
Business
More
Politics
过去 7 天
时间不限
过去 1 小时
过去 24 小时
过去 30 天
按时间排序
按相关度排序
1 小时
Janux Therapeutics Announces Proposed Public Offering
BofA Securities, TD Cowen, Stifel, Cantor and William Blair are acting as joint book-running managers for the offering. Wedbush PacGrow, LifeSci Capital, BTIG and Jones are acting as co-managers for ...
2 小时
Merck Receives FDA Breakthrough Therapy Designation for Investigational Lung Cancer Treatment
Failed to fetch dynamically imported module: https://finance.yahoo.com/assets/_app/immutable/nodes/90.BMDkfsfZ.js ...
6 小时
on MSN
Merck gets FDA Breakthrough Therapy designation for sac-TMT
Merck (NYSE:MRK) said the FDA has granted Breakthrough Therapy designation for its antibody drug conjugate sacituzumab ...
7 小时
Merck: FDA grants Breakthrough Therapy designation to sacituzumab tirumotecan
Merck (MRK) announced that the U.S. FDA has granted Breakthrough Therapy designation to sacituzumab tirumotecan for the treatment of patients ...
Cancer Therapy Advisor
8 小时
Top Lung Cancer Research of 2024
This page includes links to articles highlighting the top lung cancer research published on Cancer Therapy Advisor in 2024.
9 小时
MRK: Sac-TMT Gets FDA Breakthrough Therapy Designation For EGFR-mutated Advanced Or ...
Merck & Co., Inc. (MRK) announced Tuesday that the U.S. Food and Drug Administration has granted Breakthrough Therapy designation to ...
红板报 on MSN
18 小时
再迎突破!复宏汉霖H药 汉斯状获批非鳞状非小细胞肺癌新适应症
2024年12月3日,上海——复宏汉霖(2696.HK)宣布,公司自主研发的创新型抗PD-1单抗H药 汉斯状(通用名:斯鲁利单抗注射液)正式获得国家药品监督管理局(NMPA)批准,联合培美曲塞和卡铂适用于表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性的不可手术切除的局部晚期或转移性非鳞状非小细胞肺癌(nsNSCLC)的一线治疗。这是H药在中国获批的第五项适应症,也是继鳞状 ...
1 天
Summit Therapeutics Stock Set To Soar By Mid-2025 On HARMONi Phase 3 Trial
Summit Therapeutics shows promising results in Phase III trials for ivonescimab as a potential treatment for advanced NSCLC.
Targeted Oncology
1 天
November 2024 FDA Updates: Key Developments in Oncology
The FDA granted approval to nilotinib (Danziten) on November 14, 2024, for the treatment of adult patients with newly ...
BioSpace
1 天
AstraZeneca/Daiichi Sankyo, BioNTech, Merus to Present Promising Cancer Therapies at ESMO ...
At the conference, AstraZeneca and Daiichi Sankyo will present their case for Dato-DXd in NSCLC, while BioNTech and Merus ...
News Medical
1 天
How Dysregulated Cell Signaling Causes Disease
Dysregulated cell signaling underlies various diseases, emphasizing the importance of understanding these pathways for ...
pharmaphorum
4 天
Kelun's MSD-partnered TROP2 drug gets first okay in China
Kelun-Biotech has become the second drugmaker to bring a TROP2-directed antibody-drug conjugate to regulatory approval, ...
一些您可能无法访问的结果已被隐去。
显示无法访问的结果
反馈