等待开盘 06-25 09:30:00 美东时间
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The US FDA has approved Gilead Sciences' (GILD) Trodelvy (sacituzumab govitecan) as a first-line treatment as monotherapy and in combination with Merck's (MRK) Keytruda (pembrolizumab) for triple-nega...
今天 04:37
Moderna (MRNA) snapped a six-session winning streak on Monday, with shares falling 6.10% to $60.06 in afternoon trading. Despite the decline, the stock has been one of the market's standout performers...
06-23 02:05
A US FDA advisory panel unanimously agreed that the benefits of Moderna's (MRNA) mRNA seasonal flu vaccine, mRNA-1010, outweigh the risks in individuals 50-75 years old. The agency's Vaccines and Rela...
06-19 05:00
U.S. vaccine maker Moderna (MRNA) is exploring investments in manufacturing facilities in Germany and is particularly interested in acquiring sites that rival BioNTech (BNTX) plans to shut down as par...
06-17 15:19
Moderna (MRNA) on Tuesday said that Ester Banque, a former senior executive at Zoetis (ZTS) and Bristol Myers (BMY), will join the company as chief commercial officer as part of organizational changes...
06-16 20:57
• CMS拟议的药品价格谈判影响了默克未来的营收。 • 肿瘤学试验中的研发管线受挫,引发了市场对增长前景的担忧。 • 除息日因素也导致了股价的下跌。
06-15 18:16
Merck (NYSE:MRK), known as MSD outside of the United States and Canada, and Gilead Sciences, Inc. (NASDAQ:GILD) today announced the discontinuation of the Phase 3 KEYNOTE-D46/EVOKE-03 study investigating Gilead's
06-09 04:31
Moderna (MRNA) and Merck (MRK) said that the experimental cancer vaccine intismeran autogene plus Keytruda (pembrolizumab) led to a 49% decline in the risk of recurrence or death, and a 50% reduction ...
06-02 04:53
Tempus has been building novel biological foundation models and agentic workflows by leveraging its more than 500 petabytes of rich, molecularly grounded data—more than 45 million total de-identified patient journeys,
05-29 21:17
Merck wins EU CHMP backing for Keytruda-Padcev in cisplatin-ineligible bladder cancer EU drug regulators issued a positive CHMP opinion for Keytruda with Padcev as perioperative therapy for cisplatin-ineligible adults with resectable muscle-invasive bladder cancer. The European Commission is reviewi
05-22 19:55