Alvotech Receives EU Marketing Authorization for AVT03, a Biosimilar to Prolia and Xgeva
ByAinvest
Monday, Nov 24, 2025 5:31 am ET1min read
ALVO--
Alvotech has received marketing authorization in Europe for AVT03, a biosimilar of Prolia and Xgeva, which contain the active ingredient denosumab. The biosimilar is used to treat bone loss and osteoporosis, and has a market value of approximately $150 million in the last 12 months. The company plans to increase access to these medications by offering a lower-cost alternative. The biosimilar will be marketed by Alvotech's partners STADA and Dr. Reddy's Laboratories.

Stay ahead of the market.
Get curated U.S. market news, insights and key dates delivered to your inbox.
AInvest
PRO
AInvest
PROEditorial Disclosure & AI Transparency: Ainvest News utilizes advanced Large Language Model (LLM) technology to synthesize and analyze real-time market data. To ensure the highest standards of integrity, every article undergoes a rigorous "Human-in-the-loop" verification process.
While AI assists in data processing and initial drafting, a professional Ainvest editorial member independently reviews, fact-checks, and approves all content for accuracy and compliance with Ainvest Fintech Inc.’s editorial standards. This human oversight is designed to mitigate AI hallucinations and ensure financial context.
Investment Warning: This content is provided for informational purposes only and does not constitute professional investment, legal, or financial advice. Markets involve inherent risks. Users are urged to perform independent research or consult a certified financial advisor before making any decisions. Ainvest Fintech Inc. disclaims all liability for actions taken based on this information. Found an error?Report an Issue

Comments
No comments yet