Sandoz receives European Commission approval for Wyost and Jubbonti, the first and only biosimilars of denosumab in Europe


22 May 2024 - EC approval based on robust development program confirming that biosimilar matches reference medicine in terms of safety, efficacy and quality.

Sandoz today announced that the European Commission has granted marketing authorisation for Wyost (denosumab) and Jubbonti (denosumab), the first and only biosimilar versions of reference medicines Xgeva and Prolia in Europe.

Read Sandoz press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Biosimilar