Sandoz: Marketing authorization for Wyost and Jubbonti in the EU
Both products have been approved in the European Union for all indications of the reference medicines, namely cancer-related bone diseases for Wyost and osteoporosis for Jubbonti.
This approval is based on a solid development program confirming that these biosimilars match the reference medicines in terms of safety, efficacy and quality. Sandoz plans to launch them from November 2025.
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