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2 天
US FDA approves GE HealthCare's diagnostic drug for heart disease
The U.S. Food and Drug Administration approved GE HealthCare's diagnostic drug for use in detection of coronary artery ...
2 天
Bristol Myers wins US FDA approval for new type of schizophrenia drug
The U.S. Food and Drug Administration approved Bristol Myers Squibb's schizophrenia drug late on Thursday, making it the ...
1 天
The American Drug Mules Smuggling Fentanyl Into the U.S.
Mexican drug cartels are turning thousands of Americans into fentanyl smugglers, sending an army of couriers who can easily ...
3 天
on MSN
US FDA approves Bristol Myers' schizophrenia drug
The U.S. FDA approved Bristol Myers Squibb's schizophrenia drug on Thursday, providing patients with a treatment option that ...
2 小时
Mexican cartels flood US with fentanyl, causing 200+ deaths daily
In 2024 alone, 37.7 million pills and more than 5,400 pounds of fentanyl powder have been seized – enough to produce 269 ...
2 天
US FDA approves Sanofi-Regeneron's Dupixent for 'smoker's lung'
Sanofi recorded 10.72 billion euros ($11.94 billion) in sales for Dupixent in 2023, which includes Regeneron's share.
BioWorld
2 天
US FDA clears Cobenfy, first new schizophrenia drug in decades
The FDA has approved Cobenfy, a dual M1/M4 muscarinic agonist that offers a fundamentally different approach to treating ...
U.S. News & World Report
3 天
US FDA Approves GE HealthCare's Diagnostic Drug for Heart Disease
US FDA Approves GE HealthCare's Diagnostic Drug for Heart Disease (Reuters) - The U.S. Food and Drug Administration approved GE HealthCare's diagnostic drug for use in detection of coronary artery ...
4 天
FDA咨询委员会将聚焦施贵宝(BMY.US)和默沙东(MRK.US)的检查点抑制剂
智通财经APP获悉,9月26日,美国FDA顾问小组将重点讨论施贵宝(BMY.US)的Opdivo (nivolumab)和默沙东(MRK.US)的Keytruda ...
2 天
on MSN
Bristol Myers Gets US Nod for First New Schizophrenia Drug Type in Decades
Bristol Myers Squibb Co. gained US approval for the first new type of schizophrenia drug in seven decades, opening a fresh ...
2 天
百时美施贵宝(BMY.US)重磅抗精神病药物获批 带动股价盘前大涨
智通财经APP获悉,美国食品和药物管理局(FDA)周四批准了由美国医药巨头百时美施贵宝公司(BMY.US)开发的Cobenfy(xanomeline以及trospium ...
5 天
诺华制药(NVS.US)创新放射性疗法Pluvicto在华拟纳入优先审评 治疗前列腺癌
2022年3月,诺华宣布FDA已经批准该公司的Pluvicto上市,用于治疗PSMA阳性转移性去势抵抗性前列腺癌 ...
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