Welcome to our dedicated page for Kodiak Sciences news (Ticker: KOD), a resource for investors and traders seeking the latest updates and insights on Kodiak Sciences stock.
Kodiak Sciences Inc. (Nasdaq: KOD) is a precommercial, retina-focused biotechnology company whose news flow centers on clinical trial progress, scientific data presentations and capital markets activity. The company is developing biologic therapeutics for retinal vascular diseases and macular edema secondary to inflammation (MESI), built on its proprietary ABC Platform and late-stage programs tarcocimab, KSI-501 and KSI-101.
On this page, readers can follow news about Kodiak’s Phase 3 studies, including GLOW2 in diabetic retinopathy, DAYBREAK in wet age-related macular degeneration, and the PEAK and PINNACLE studies in MESI. Company press releases describe milestones such as completion of enrollment in pivotal trials, new data from the Phase 1b APEX study of KSI-101, and updates on the performance of tarcocimab and KSI-501 in retinal vascular indications.
Kodiak Sciences also issues news about participation in major scientific and investor conferences, where its management and clinical collaborators present data on retinal programs and discuss the potential of IL-6 and VEGF targeting in eye disease. In addition, investors will find announcements related to public offerings of common stock and other financing activities, which the company uses to support its late-stage development and manufacturing efforts.
For anyone tracking KOD stock or developments in retinal biotechnology, this news feed offers a centralized view of Kodiak Sciences’ clinical, scientific and corporate updates as it advances its portfolio of investigational retinal medicines.
Kodiak Sciences announced the treatment of the first patients in the Phase 3 GLOW2 study of tarcocimab tedromer for diabetic retinopathy (DR) on May 13, 2024. This follows the successful GLOW1 study, where tarcocimab improved DR by 29-fold in 2-step DRSS improvement and reduced sight-threatening complications by 89% over 48 weeks. GLOW2, with extended dosing intervals including 6-month dosing for all patients, aims to finish enrollment by year-end. The study anticipates mirroring GLOW1 results, potentially leading to marketing authorization for tarcocimab in treating DR.
Kodiak Sciences Inc. announced scientific presentations on its clinical pipeline programs at ARVO 2024, highlighting the efficacy and safety of tarcocimab and KSI-501 in diabetic retinopathy patients. The ABC Platform shows potential for targeted, high drug-antibody-ratio conjugates. The company aims to address unmet needs in retinal diseases with innovative therapeutic candidates.
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