Glaukos Announces Positive Topline Outcomes in Phase 3 Confirmatory Trial for Epioxa™, Achieving Primary Efficacy Endpoint and Demonstrating Favorable Tolerability and Safety
Glaukos Corporation (GKOS)
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Source: Business Wire
Phase 3 Confirmatory Trial Met Pre-Specified Primary Efficacy Endpoint and Demonstrated Excellent Tolerability and a Favorable Safety Profile Through 12 Months, Supporting Anticipated New Drug Application (NDA) Submission by End of 2024Data Suggest Epioxa Has the Potential to Provide the Ophthalmic Community and Patients with the First FDA-Approved, Non-Invasive Drug Therapy Alternative for Keratoconus 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 that the second Phase 3 confirmatory pivotal trial for Epioxa™ (Epi-on), its next-generation corneal cross-linking iLink therapy for the treatment of keratoconus, successfully met the study’s pre-specified primary efficacy endpoint, demonstrating a clinically relevant and statistically significant improvement in maximum corneal curvature (Kma
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GKOS
Earnings
- 11/4/24 - Beat
GKOS
Sec Filings
- 11/15/24 - Form 8-K
- 11/14/24 - Form SC
- 11/5/24 - Form 10-Q
- GKOS's page on the SEC website