Alvotech announced that its biosimilar to Eylea®, AVT06, has received regulatory approval from the European Commission for marketing in the European Economic Area as of August 21, 2025. Additionally, the UK Medicines and Healthcare products Regulatory Agency (MHRA) approved AVT06 for marketing in the UK on August 28, 2025. These approvals pave the way for the commercial launch of AVT06 in Europe and the UK following the expiry of the Supplementary Protection Certificates for Eylea® on November 23, 2025.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Alvotech SA published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001137861-en) on November 10, 2025, and is solely responsible for the information contained therein.
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