March 26 (Reuters) - FRESENIUS SE & CO KGAA FREG.DE:
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)
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