||||||||||licaminlimab (OCS-02) / Oculis Biomarker, Journal: Pharmacogenomic Analysis of Response to Topical Tumor Necrosis Factor ? Antagonist Licaminlimab (OCS-02) in Dry Eye Disease. (Pubmed Central) - Feb 28, 2024 The CC genotype of rs1800693, relatively common in patients with DED, was strongly associated with response to licaminlimab and decreased inflammatory cytokine gene expression in ocular surface cells during treatment. This study is one of the first to our knowledge to investigate pharmacogenomics in the treatment of DED.
||||||||||licaminlimab (OCS-02) / Oculis Trial initiation date, Trial primary completion date: RELIEF: Safety and Efficacy of Licaminlimab Ophthalmic Suspension for the Treatment of Dry Eye Disease (clinicaltrials.gov) - Nov 28, 2023 P2, N=120, Not yet recruiting, Sponsor: Oculis Not yet recruiting --> Recruiting Initiation date: Aug 2023 --> Dec 2023 | Trial primary completion date: Aug 2024 --> May 2024
||||||||||OCS-02 / Oculis Clinical, P2 data: Topical Anti-TNFα Agent Licaminlimab (OCS-02) Relieves Persistent Ocular Discomfort in Severe Dry Eye Disease: A Randomized Phase II Study. (Pubmed Central) - Jul 14, 2022 Serum licaminlimab was undetectable in most patients; the maximum concentration observed was 8.47 ng/mL. Topical ocular licaminlimab demonstrated statistically significant improvement in global ocular discomfort score compared to Vehicle in patients with severe DED, with good tolerability, no increase in IOP, and minimal systemic drug exposure.
||||||||||licaminlimab (OCS-02) / Oculis Trial completion: Proof of Concept Study to Evaluate Safety and Efficacy of LME636 in the Treatment of Acute Anterior Uveitis (clinicaltrials.gov) - Apr 6, 2016 P2, N=46, Completed, Sponsor: Alcon Research Topical ocular licaminlimab demonstrated statistically significant improvement in global ocular discomfort score compared to Vehicle in patients with severe DED, with good tolerability, no increase in IOP, and minimal systemic drug exposure. Active, not recruiting --> Completed