*FRESENIUS SE - RECEIVES FDA APPROVAL FOR THEIR DENOSUMAB BIOSIMILARS AND SECURES GLOBAL SETTLEMENT
*FRESENIUS SE - DENOSUMAB BIOSIMILARS ARE APPROVED FOR ALL INDICATIONS OF THE REFERENCE PRODUCTS PROLIA®* (DENOSUMAB) AND XGEVA®* (DENOSUMAB), RESPECTIVELY
*FRESENIUS SE - FRESENIUS’ OPERATING COMPANY REACHED GLOBAL SETTLEMENT WITH AMGEN, ALLOWING LAUNCH OF THESE BIOSIMILARS IN THE US FROM MID-2025 AND IN EUROPE LATER IN H2 OF 2025
*Further company coverage: FREG.DE
* (Gdansk Newsroom)
* ((Gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))
((Reuters Investor Briefs; email: reutersinvestor.briefs@thomsonreuters.com))
Source Date/Time = 26-MAR-202516:00:00.487 GMT