Kodiak Sciences Reports Positive Vision Gains from Macular Edema Drug.
PorAinvest
lunes, 15 de septiembre de 2025, 8:11 am ET1 min de lectura
KOD--
The APEX study, which included patients with macular edema secondary to inflammation, demonstrated that KSI-101 resulted in a significant improvement in best-corrected visual acuity (BCVA) and retinal thickness. Specifically, over 60% of patients in the top two dose levels (5 mg and 10 mg) achieved a 3-line or more gain on the eye chart, equivalent to a 15-letter gain. Additionally, a majority of patients achieved resolution of intra-retinal and sub-retinal fluid, with over 90% showing retinal dryness by week 8.
The Phase 3 PEAK and PINNACLE studies, which are currently enrolling patients, will further evaluate KSI-101's efficacy and safety. These studies will test the top two dose levels of KSI-101 in patients with MESI, comparing it to sham treatment. The primary and key secondary endpoints will be evaluated at week 24.
KSI-101 is a bispecific protein targeting interleukin-6 (IL-6) and vascular endothelial growth factor (VEGF), making it a potent and high-strength therapy. The company's focus is on continuing the enrollment of patients into the PEAK and PINNACLE studies.
Kodiak Sciences, a precommercial retina-focused biotechnology company, is committed to researching, developing, and commercializing transformative therapeutics. The company's ABC Platform uses molecular engineering to merge protein-based and chemistry-based therapies, and it is developing a portfolio of three late-stage clinical programs, including KSI-101.
Kodiak Sciences reported new data showing "meaningful" vision gains from its macular edema drug, tarcocimab. The company's Antibody Biopolymer Conjugate (ABC) Platform is a technology platform for retinal medicines. Tarcocimab is an anti-VEGF antibody biopolymer conjugate under development for diabetic retinopathy and wet age-related macular degeneration. Kodiak is also developing KSI-501, a bispecific antibody biopolymer conjugate targeting IL-6 and VEGF, and KSI-101, an unconjugated bispecific protein targeting IL-6 and VEGF.
Kodiak Sciences Inc. (Nasdaq: KOD) has reported promising new data from its Phase 1b APEX study on KSI-101, a novel investigational therapy for macular edema secondary to inflammation (MESI). The study, presented at the Retina Society's 58th Annual Scientific Meeting in Chicago, showed that KSI-101 achieved clinically meaningful vision gains and rapid retinal drying in patients with MESI.The APEX study, which included patients with macular edema secondary to inflammation, demonstrated that KSI-101 resulted in a significant improvement in best-corrected visual acuity (BCVA) and retinal thickness. Specifically, over 60% of patients in the top two dose levels (5 mg and 10 mg) achieved a 3-line or more gain on the eye chart, equivalent to a 15-letter gain. Additionally, a majority of patients achieved resolution of intra-retinal and sub-retinal fluid, with over 90% showing retinal dryness by week 8.
The Phase 3 PEAK and PINNACLE studies, which are currently enrolling patients, will further evaluate KSI-101's efficacy and safety. These studies will test the top two dose levels of KSI-101 in patients with MESI, comparing it to sham treatment. The primary and key secondary endpoints will be evaluated at week 24.
KSI-101 is a bispecific protein targeting interleukin-6 (IL-6) and vascular endothelial growth factor (VEGF), making it a potent and high-strength therapy. The company's focus is on continuing the enrollment of patients into the PEAK and PINNACLE studies.
Kodiak Sciences, a precommercial retina-focused biotechnology company, is committed to researching, developing, and commercializing transformative therapeutics. The company's ABC Platform uses molecular engineering to merge protein-based and chemistry-based therapies, and it is developing a portfolio of three late-stage clinical programs, including KSI-101.

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios