Kodiak Sciences to Present at Innovate Retina 2024
Presentation and Panel details are below:
- Presentation Title: Update on Antibody Biopolymer Conjugates: Optimizing Immediacy and Durability
Time:3:30 PM CT
Presenter:Mark Barakat , M.D., FASRS, Clinical Assistant Professor of Ophthalmology,University of Arizona College of Medicine –Phoenix ; Founder and Director of Research,Retina Macula Institute of Arizona ; Medical Director,Spectra Eye Institute - Panel Title: The Future of Retinal Therapeutics
Time:6:30 PM CT
Kodiak Panelist:Victor Perlroth , M.D., Chairman and Chief Executive Officer
Slides of the presentation will be made available on the "Events and Presentations" section of Kodiak's website at http://ir.kodiak.com/ at the beginning of the presentation.
About
Kodiak's lead investigational medicine, tarcocimab, is a novel anti-VEGF antibody biopolymer conjugate under development for the treatment of high prevalence retinal vascular diseases. Tarcocimab is currently being studied in two Phase 3 clinical trials, GLOW2 in patients with diabetic retinopathy and DAYBREAK in patients with wet AMD. Both studies are actively enrolling patients.
KSI-501 is our second investigational medicine, a first-in-class anti-IL-6, VEGF-trap bispecific antibody biopolymer conjugate designed to inhibit both IL-6 mediated inflammation and VEGF-mediated angiogenesis and vascular permeability. KSI-501 is being developed for the treatment of high prevalence retinal vascular diseases to address the unmet needs of extended durability and targeting multiple disease biologies for differentiated efficacy. The Phase 3 DAYBREAK study of KSI-501 in wet AMD is actively enrolling patients.
KSI-101, our third product candidate, is a novel anti-IL-6, VEGF-trap bispecific protein. Kodiak is developing KSI-101 for the treatment of retinal inflammatory diseases, as currently there are no available intravitreal biologic therapies addressing the spectrum of inflammatory conditions of the retina. The Phase 1b APEX study of KSI-101 is actively enrolling patients, as a precursor to activating the Phase 2b/3 PEAK and PINNACLE studies in patients with macular edema secondary to inflammation (MESI).
For more information, please visit www.kodiak.com.
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SOURCE
Kodiak Contact: John Borgeson, Chief Financial Officer, Tel (650) 281-0850, ir@kodiak.com