The FDA has approved two new denosumab biosimilars that are interchangeable with the reference medications Prolia and Xgeva, ...
The fourth pair of denosumab biosimilars, Conexxence and Bomyntra, are expected to launch in the United States in mid 2025, ...
Net prices that health plans paid for medicines rose a modest 0.4% in the fourth quarter, but that compared unfavorably with ...
The formulation comparison between a biosimilar and a branded biologic. The cost, availability, and supply chain benefits of ...
The inquiry is the latest effort by the European Commission and European countries to scrutinize potential antitrust behavior ...
AbbVie’s Humira was the top-selling drug in the world for many years. Now, its sales are eroding as doctors switch to ...
10d
The Chosun Ilbo on MSNKorean biotech firms race into $26 billion U.S. biosimilar marketSouth Korean biotech firms are targeting the $26 billion biosimilar market opening up as patents expire on more than 10 ...
On March 26, 2025, the FDA approved Fresenius Kabi’s denosumab biosimilars, CONEXXENCE® (denosumab-bnht) and BOMYNTRA® (denosumab-bnht), ...
Fresenius announced that the Biologics License Application (BLA) for the denosumab biosimilars Conexxence® (denosumab-bnht) and Bomyntra® (denosumab-bnht) of its operating company Fresenius Kabi, has ...
The acquisition in brief "Alvotech has a best-in-class biosimilars manufacturing site in Iceland, both for drug substance and drug products. At the same time, our strong in-house R&D capabilities have ...
HYDERABAD: Dr Reddy’s Labs on Wednesday said its subsidiary, Dr Reddy’s Labs SA, has entered into commercialisation and ...
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