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Glaukos Announces FDA Acceptance of NDA Submission for Epioxa™

1. Glaukos gets FDA Day 74 NDA notice for Epioxa therapy. Regulatory step marks product pipeline progress.

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Why Bullish?

The FDA notification signals progress in Glaukos’ pipeline, echoing past biotech milestones that led to positive price reactions.

How important is it?

This FDA milestone can boost investor confidence by advancing Epioxa towards market approval, influencing near-term revenue potential.

Why Short Term?

Regulatory milestones often trigger immediate investor optimism and price volatility, as seen in similar NDA events.

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ALISO VIEJO, Calif.--(BUSINESS WIRE)--Glaukos Corporation (NYSE: GKOS), an ophthalmic pharmaceutical and medical technology company focused on novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases, today announced it has received the “Day 74” notification from the U.S. Food and Drug Administration (FDA) acknowledging the previously submitted New Drug Application (NDA) for Epioxa™ (Epi-on), its next-generation corneal cross-linking iLink therapy for the treatment.

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