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The EU approved Alvotech’s denosumab biosimilar for osteoporosis and cancer-related bone issues, boosting treatment access and lowering costs.
The European Commission has approved Alvotech’s biosimilar AVT03, a denosumab alternative, for treating osteoporosis and preventing bone complications in advanced cancer patients across the EEA, Switzerland, and the UK.
Approved based on extensive data confirming safety and efficacy, AVT03 will be marketed by STADA and Dr. Reddy’s under the brands Kefdensis®, Zvogra®, Acvybra®, and Xbonzy®.
The move aims to expand access to critical treatments and support healthcare cost sustainability.
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La UE aprobó el biosimilar de denosumab de Alvotech para la osteoporosis y problemas óseos relacionados con el cáncer, aumentando el acceso al tratamiento y reduciendo los costos.