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  • Alteogen secures EU authorization for Eylea biosimilar
  • by Cha, Jihyun | translator Alice Kang | Sep 18, 2025 06:03am
Secures marketing authorization from the European Commission for its Eylea Biosimilar
¡°For Use in Age-Related Macular Degeneration and Diabetic Macular Edema¡±
[Bio platform company Alteogen (CEO Soon-jae Park) announced on the 17th that it has obtained marketing authorization from the European Commission (EC) for ¡®Eyluxvi (project name ALT-L9),¡¯ an Eylea biosimilar it had jointly developed with Alteogen Biologics.

Eyluxvi is Alteogen¡¯s second biosimilar product to receive approval, following its Herceptin biosimilar. The final authorization was granted about two months after the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive opinion in July.

Eylea is a widely used treatment for ophthalmic diseases such as wet age-related macular degeneration (wAMD) and diabetic macular edema (DME). In 2024, it generat
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