Core Insights - EyePoint Pharmaceuticals reported significant progress in its Phase 3 trials for DURAVYU, with over 90% patient enrollment in the LUGANO trial and over 50% in the LUCIA trial, aiming for completion in the second half of 2025 [2][4][5] - The company achieved total net revenue of 24.5millionforQ12025,asubstantialincreasefrom11.7 million in Q1 2024, primarily driven by license and royalty income [6][7] - Operating expenses rose to 73.3millioninQ12025,upfrom45.0 million in the prior year, largely due to costs associated with the ongoing clinical trials [8] Financial Performance - Total net revenue for Q1 2025 was 24.5million,comparedto11.7 million in Q1 2024, with net product revenue remaining stable at 0.7million[6][7]−Licenseandroyaltyrevenueincreasedto23.7 million in Q1 2025 from 11.0millioninthesameperiodin2024,attributedtodeferredrevenuerecognitionfromtheout−licenseofYUTIQ[7]−ThenetlossforQ12025was45.2 million, or (0.65)pershare,comparedtoanetlossof29.3 million, or (0.55)pershare,inQ12024[8][20]ResearchandDevelopmentHighlights−DURAVYU′sPhase2VERONAtrialindiabeticmacularedema(DME)demonstratedsignificantefficacy,withaBCVAimprovementof+10.3letterscomparedto+3.0lettersforafliberceptcontrolatweek24[5][14]−Thecompanyhasastrongcashpositionof318 million as of March 31, 2025, which is expected to fund operations into 2027, beyond the anticipated topline data for the Phase 3 trials [4][10] - DURAVYU is positioned as a potential first-to-market treatment for wet AMD, with a robust safety and efficacy profile supported by ongoing clinical trials [2][5][12]