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.
1. Glaukos gets FDA Day 74 NDA notice for Epioxa therapy. Regulatory step marks product pipeline progress.
The FDA notification signals progress in Glaukos’ pipeline, echoing past biotech milestones that led to positive price reactions.
This FDA milestone can boost investor confidence by advancing Epioxa towards market approval, influencing near-term revenue potential.
Regulatory milestones often trigger immediate investor optimism and price volatility, as seen in similar NDA events.