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The U.S. launch of Conexxence and Bomyntra follows the FDA’s approval in March 2025.
July 1, 2025
By: Rachel Klemovitch
Assistant Editor
Fresenius announced that its operating company, Fresenius Kabi, has introduced two new biosimilars – Conexxence (denosumab-bnht) and Bomyntra (denosumab-bnht) – in the United States. These denosumab biosimilars are approved by the FDA for all indications of the reference products: Prolia (denosumab) and Xgeva (denosumab), respectively. Conexxence (denosumab-bnht) is approved for use in various adult patient populations at high risk for fractures, including individuals with oste...
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