Oculis Completes Randomization in PREDICT-1 Registrational Trial of Licaminlimab for TNFR1-Mediated Dry Eye Disease
Globe Newswire•19/10/2026•02:00 ET
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Key Highlights
- ➤176 patients randomized in Oculis’ PREDICT-1 registrational dry-eye trial
- ➤Two-thirds of enrolled patients carry the specified TNFR1 genetic variant
- ➤Topline PREDICT-1 results expected around year-end 2026
- ➤Licaminlimab targets an estimated 1.3–1.9 million U.S. patients with the variant
- ➤Prior Phase 2 trial showed statistically significant ocular-discomfort reduction at Day 29
Expert Statements
Riad Sherif, Chief Executive Officer of Oculis
“Completing randomization in such a timeframe with a new modality demonstrates that genotype-driven development is crucial and precision medicine is urgently needed in DED. PREDICT-1 is an important operational milestone as we track toward topline results around year-end 2026. In prior Phase 2 studies, Licaminlimab showed robust improvement across both signs and symptoms of dry eye disease, with an amplified response in patients harboring a specific TNFR1 genotype. Importantly, a simple, non-invasive genetic biomarker test can identify this patient population, supporting the practical application of this precision medicine approach. PREDICT-1 builds directly on that scientific rationale to validate our genotype-guided strategy. If successful, Licaminlimab has the potential to pioneer a first-in-class precision medicine treatment paradigm, delivering targeted relief to a large, underserved patient population with TNFR1-driven disease.”
Anat Galor, Professor of Ophthalmology, Bascom Palmer Eye Institute, Miami
“Dry eye disease is a highly heterogeneous condition, and treatment response can vary considerably between patients. As a result, selecting the right therapy often involves a lengthy trial-and-error process that can lead to patient dissatisfaction and early treatment discontinuation. A precision medicine approach to identify individuals more likely to benefit from a specific therapy could meaningfully advance care for both patients and clinicians. The findings observed in earlier studies of Licaminlimab provide a compelling rationale for the PREDICT-1 trial, and I look forward to seeing whether this targeted approach can advance a more effective treatment paradigm and improve outcomes for patients living with dry eye disease.”
High-Responder Target Enrichment: 2/3 of the 176 enrolled patients carry the target TNFR1 genetic variant previously linked to enhanced clinical response in Phase 2 trials
Precision Medicine Approach in a Large Market: Licaminlimab is positioned as a potential first-in-class precision medicine for an estimated 1.5+ million patients in the U.S. with moderate-to-severe TNFR1-mediated dry eye disease (DED)(1-4), addressing a critical unmet need in a historically heterogeneous indication.
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