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Regeneron submits BLA for VEGF Trap-Eye in wet AMD, but investors unimpressed

This article was originally published in Scrip

Executive Summary

Although Regeneron Pharmaceuticals submitted its biologics license application (BLA) to the US FDA for its VEGF Trap-Eye (aflibercept) as a treatment for wet age-related macular degeneration (AMD) a month ahead of analysts' expectations, apparently investors 22 February did not view that accomplishment as a pleasant surprise.



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