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
时间不限
过去 1 小时
过去 24 小时
过去 7 天
过去 30 天
按时间排序
按相关度排序
1 天
MAI Capital Management Has $501,000 Holdings in Sanofi (NASDAQ:SNY)
MAI Capital Management decreased its stake in Sanofi (NASDAQ:SNY – Free Report) by 38.2% during the 3rd quarter, ...
Managed Healthcare Executive
3 天
New Advertising Campaign Aims to Raise Awareness of Chronic Hand Eczema
The top spenders in the space, however, are Sanofi and Regeneron. The companies marketed Dupixent (dupilumab), a biologic ...
Future Market Insights
5 天
Global Injection Pen Market Set to Soar, Projected to Reach USD 85.8 Billion by 2033
Injection Pen Market. The global injection pen market is on track for substantial growth, with a forecasted compound annual ...
5 天
10 Best Genomics Stocks To Buy Right Now
Best Genomics Stocks To Buy Right Now. Genomics is the study of genes and how they function. Many rapidly growing companies ...
Medscape
5 天
Dupilumab Beneficial When Antihistamines Fall Short for Chronic Spontaneous Urticaria
Dupilumab (Dupixent), a fully human monoclonal antibody that targets the interleukin (IL)-4 and IL-13 pathways, is currently ...
6 天
FDA Accepts SNY and REGN's Dupixent Re-Submitted sBLA for Urticaria
The FDA is set to give its decision on SNY and REGN's sBLA for Dupixent for chronic spontaneous urticaria on April 18, 2025.
FiercePharma
6 天
Sanofi lays out €40M to beef up transplant, diabetes drug production in France
With several high-profile manufacturing outlays already in the books in Europe this year, Sanofi is returning to the bloc in ...
The Pharma Letter
7 天
FDA accepts Dupixent sBLA resubmission for CSU
The US Food and Drug Administration (FDA) has accepted for review the resubmission of the supplemental Biologics License ...
Daily
7 天
Sanofi, Regeneron Dupixent sBLA accepted for USFDA review for chronic spontaneous urticaria
Paris: Sanofi and Regeneron has announced that the US Food and Drug Administration (FDA) has accepted for review the ...
Monthly Prescribing Reference
9 天
FDA to Review Resubmitted Dupilumab sBLA for Chronic Spontaneous Urticaria
The resubmitted sBLA will include results from Study C, which evaluated biologic-naive patients with uncontrolled CSU on antihistamines.
9 天
FDA reviews Sanofi and Regeneron’s Dupixent label expansion for urticaria
The FDA has accepted Sanofi and Regeneron’s application to expand Dupixent’s use, with a decision expected by April 2025.
Managed Healthcare Executive
9 天
FDA Sets Date For Resubmitted Dupixent in Inflammatory Skin Disease
The FDA has provided a date of April 18, 2025, to review the application for Dupixent to treat patients with chronic ...
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