The US Food and Drug Administration (FDA) has approved Celltrion’s biosimilars referencing Amgen’s bone disease therapy ...
The FDA has approved two new biosimilars of denosumab for all indications of the reference medications Prolia and Xgeva, ...
Four biosimilars for Stelara have launched in the United States this year following legal settlements with the reference ...
The company's vice president and general manager of U.S. business operations explains how Amgen is going to deliver on its ...
South Korea-based Celltrion today announced that the US Food and Drug Administration (FDA) has approved Stoboclo and Osenvelt ...
Below, we can observe the evolution of the volume and open interest of calls and puts, respectively, for all of Amgen's whale ...
Johnson & Johnson on Monday filed a lawsuit against Samsung Bioepis in a New Jersey federal court, accusing the Korean ...
Regeneron recently announced it would initiate a quarterly dividend of $0.88, a competitive amount for a company first ...
biosimilars for all indications of reference products PROLIA (denosumab) and XGEVA (denosumab) respectively, from Amgen Inc. (AMGN). In accordance with a settlement agreement with Amgen ...
Celltrion has received permission from the Food and Drug Administration for Stoboclo (CT-P41, denosumab-bmwo) and Osenvelt ...
Amgen (AMGN) reported earnings 30 days ago. What's next for the stock? We take a look at earnings estimates for some clues.
On March 3, 2025, the FDA approved Celltrion’s denosumab biosimilars, STOBOCLO® (denosumab-bmwo; 60 mg/mL injection) and OSENVELT® (denosumab-bmwo; ...
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