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Kodiak Sciences

NASDAQ: KOD ↗$93.24 USD

Kodiak Sciences is a precommercial, retina-focused biotechnology company based in Palo Alto, California, built around its Antibody Biopolymer Conjugate (ABC) platform, which conjugates a humanised anti-VEGF antibody to a high-molecular-weight phosphorylcholine-based biopolymer through a single-site covalent linkage to extend durability of effect in the eye. Its lead medicine, Zenkuda (tarcocimab tedromer), reported positive topline results in the pivotal Phase 3 DAYBREAK study in wet age-related macular degeneration on September 28, 2026, meeting its primary endpoint at a p-value of 0.0007 with non-inferior vision gains versus aflibercept at year one and 54% of patients on six-month dosing durability, and now has a BLA-ready profile across five positive Phase 3 studies. The company plans a multi-indication Biologics License Application in the fourth quarter of 2026 spanning wet AMD, diabetic retinopathy and retinal vein occlusion, while its bispecific VEGF/IL-6 inhibitor tabirafusp alfa tedromer (KSI-501) is being evaluated in wet AMD and diabetic macular edema.

Company Info

Sector:Biotechnology / Ophthalmology (Retinal Therapeutics)
Headquarters:Palo Alto, California, USA
Founded:2009
Website:kodiak.com/

Upcoming Milestones & Key Dates

Q4 2026
Regulatory

Planned multi-indication BLA submission for Zenkuda covering DAYBREAK and DAYLIGHT (wet AMD), GLOW and GLOW2 (diabetic retinopathy) and BEACON (retinal vein occlusion)

Q4 2026
Clinical

Post-hoc analyses planned to identify treatment-naive wet AMD patient sub-groups that benefit from IL-6 inhibition

Clinical Development Pipeline

Zenkuda (tarcocimab tedromer)

Target: VEGF-A (anti-VEGF Antibody Biopolymer Conjugate)
Wet AMD, diabetic retinopathy and macular edema following retinal vein occlusion (five positive Phase 3 studies; multi-indication BLA planned Q4 2026)
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Tabirafusp alfa tedromer (KSI-501)

Target: VEGF and IL-6 bispecific antibody biopolymer conjugate
Wet AMD (met primary endpoint in Phase 3 DAYBREAK) and diabetic macular edema (Phase 3 ALTO enrolling)
Preclinical
Phase 1
Phase 2
Phase 3
Approved

KSI-101

Target: Bispecific protein
Macular edema associated with retinal vein occlusion
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

Leadership Team

Victor Perlroth, M.D.

Co-Founder, Chairman and Chief Executive Officer

John Borgeson

Chief Financial Officer

Careers & Job Openings

See all open roles

Multiple Departments
Palo Alto, CA
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