Formycon will find out in June whether its FYB203 proposed biosimilar to Eylea (aflibercept) will receive US Food and Drug Administration approval, in the wake of the agency approving last month the first biosimilars to the world’s leading anti-VEGF brand to treat wet age-related macular degeneration.
The German-based developer and its license partner Klinge Biopharma revealed last August that they had obtained a June target action...
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