Phase 3 Pivotal Trials Met Pre-Specified Primary Efficacy Endpoints for Both Doses of iDose TR (Fast- and Slow-Release Models), Supporting Anticipated Upcoming NDA Submission
93% of Slow-Release iDose TR Subjects Remained Well-Controlled on the Same or Fewer IOP-Lowering Topical Medications at 12 Months After a Single Administration of iDose TR, Including 81% Completely Free of IOP-Lowering Medications
iDose TR Demonstrated Excellent Tolerability and a Favorable Safety Profile Through 12 Months
https://finance.yahoo.com/news/glaukos-announces-positive-topline-outcomes-110000805.html
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