Summary of Oculis Holding (NasdaqGM:OCS) FY Conference Call Company Overview - Oculis is a biopharma company focused on neuro ophthalmology and ophthalmology, publicly listed on Nasdaq for two and a half years [4][2] - The company has three candidates in Phase III trials, with significant milestones expected from 2026 to 2028 [4][4] Key Assets and Mechanisms Privo Sector (Acute Optic Neuritis) - Privo Sector is a neuroprotective drug targeting acute optic neuritis, a condition often associated with multiple sclerosis (MS) [5][9] - The drug has shown promising results in preclinical and clinical trials, demonstrating neuroprotection and improved vision [16][16] - The market for acute optic neuritis is estimated to be between $6 billion to $7 billion, with no current competition [18][18] - The company plans to conduct two Phase III trials (PIONEER one and two) with a sample size of 180 to 200 patients each, expected to start recruitment within 12 months [31][31][54][54] Lecamilab (Dry Eye Disease) - Lecamilab is a TNF inhibitor targeting inflammation in dry eye disease, with a focus on a specific patient population identified by a biomarker [58][61] - The company aims to conduct a precision medicine approach, significantly reducing the patient population to 20% who are likely to respond positively to the treatment [59][61] - The ongoing PREDICT study is expected to read out results in the second half of next year [78][78] OCS O1 (Diabetic Macular Edema - DME) - OCS O1 is the first eye drop for retina in DME, currently in Phase III trials with readouts planned for Q2 next year [87][87] - The product aims to address early intervention in DME, targeting a larger patient population than currently treated [90][90] - The expected efficacy is comparable to existing treatments, with a goal of showing significant improvement in visual acuity [92][92] Financial Position - Oculis has a strong balance sheet with cash reserves expected to last until 2029, allowing the company to fund its six Phase III trials [98][98] Market Dynamics - The U.S. market for acute optic neuritis has approximately 60,000 to 70,000 patients annually, with pricing for orphan indications ranging from $100,000 to $400,000 [36][37] - The company has identified a small number of neuro-ophthalmologists (420) who will be able to prescribe its products, indicating a focused market entry strategy [38][38] Strategic Focus - Oculis plans to prioritize the Privo Sector while exploring partnerships for commercialization outside the U.S. [96][96] - The company aims to maintain a strong position before seeking partnerships, particularly after the readout of its DME trial [97][97] Conclusion - Oculis is positioned to make significant advancements in the treatment of acute optic neuritis, dry eye disease, and diabetic macular edema, with a robust pipeline and financial backing to support its clinical trials and market entry strategies [99][99]

Summary of Oculus Fireside Chat Company Overview - **Company**: Oculus - **Industry**: Ophthalmology and Neuro-Ophthalmology - **Key Focus**: Development of a diversified and unique ophthalmology pipeline addressing unmet needs in ophthalmology and neuro-ophthalmology diseases with novel assets [1][2] Core Assets 1. **OCS O1**: - Based on OptiReach technology, designed for diabetic macular edema (DME) - Targets early intervention and non-responders among the 1.8 million diagnosed patients, with only 500,000 currently treated [4][34] - Aims to address the 1.3 million patients not receiving adequate treatment [4][36] 2. **OCS O2 (Lickamimab)**: - First precision medicine for dry eye disease, targeting patients with TNF R1 genotype - Approximately 10 million patients suffer from moderate to severe dry eye, with 20% having the TNF R1 gene, showing significantly better responses [5][44] 3. **OCS O5 (Privel Sector)**: - A novel neuroprotective treatment for acute optic neuritis, an orphan disease with no current neuroprotective treatments available - Positive data from Phase 2 ACUITY trial showing biological, anatomical, and functional efficacy [6][9][11] Market Dynamics - **DME Market**: - Current treatments are invasive (anti-VEGF and steroid implants), leading to low compliance; 60% of diagnosed patients are untreated [33] - OCS O1 aims to fill the treatment void for early-stage patients and provide a non-invasive option for those already treated [34][36] - **Acute Optic Neuritis**: - Estimated 65,000 patients in the US and Europe, with no approved products currently available [20] - OCS O5 is positioned to improve low contrast visual acuity (LCVA) and preserve neuronal health [20][24] Clinical Development and Regulatory Pathways - **OCS O5**: - Moving towards registrational studies based on positive Phase 2 results, with FDA interactions planned for the second half of the year [27][28] - **OCS O1**: - Phase 3 trial ongoing with over 800 patients, expecting results in Q2 of next year [39][41] - **Dry Eye Program**: - Phase 3 study design approved by the FDA, focusing on TNF R1 positive patients with a primary endpoint of global ocular discomfort score [42][44] Upcoming Catalysts - Regulatory interactions with the FDA for OCS O5 across three indications (acute optic neuritis, MS relapses, NAION) [47] - Top-line results from the DME trial expected in Q2 of next year [48] - Dry eye study results anticipated in the second half of next year [48] Additional Insights - The company emphasizes the importance of non-invasive treatments in improving patient compliance and outcomes in ophthalmology [35][41] - The potential for OCS O5 to expand into other indications beyond acute optic neuritis, such as glaucoma, is acknowledged [18][24]