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  "documentTitle": "Oculis | Investor Presentation Deck | 48 slides",
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      "text": "N=350-400/trial\nRandomization 1:1\nOCS-01 (6x/day) / Vehicle (6x/day) for 6 weeks (Induction)\nOCS-01 (3x/day) / Vehicle (3x/day) for 46 weeks (Maintenance)",
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      "text": "N=148\nRandomization 2:1\nOCS-01 (6x/day) / Vehicle (6x/day) for 6 weeks (Induction)\nOCS-01 (3x/day) / Vehicle (3x/day) for 6 weeks (Maintenance)",
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      "text": "Oculis Diamond",
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      "text": "STAGE 2\nTWO IDENTICAL 52-wk GLOBAL PIVOTAL TRIALS INITIATED",
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      "text": "STAGE 1\nCOMPLETED\nALL COMERS: 2/3 Naïve, 1/3 Previously Treated",
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      "text": "Results determined dosing\n& sample size for Stage 2\nPrimary Endpoint:\nChange in BCVA ETDRS letter score at week 6",
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      "text": "BCVA (Best corrected visual acuity); DME (Diabetic macular edema); ETDRS (Early Treatment Diabetic Retinopathy Study).\nMulticenter Study on the Efficacy and Safety of OCS-01 in Subjects With Diabetic Macular Edema. ClinicalTrials.gov identifier: NCT05066997. Updated January 17, 2023.\nStudy of the Efficacy and Safety of OCS-01 Eye Drops in Subjects With Diabetic Macular Edema (DIAMOND-2). ClinicalTrials.gov identifier: NCT06172257. Updated December 15, 2023.",
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      "text": "Evaluating OCS-01 efficacy and safety",
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      "text": "OCS-01 | Phase 3 DIAMOND Program in DME",
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