Kodiak Sciences shares surge 178% after Zenkuda and tabirafusp-ted match Eylea in Phase 3 trial

Kodiak Sciences stock jumped 178% after its two eye drugs, Zenkuda and tabirafusp-ted, matched Regeneron’s Eylea in a Phase 3 trial for wet age-related macular degeneration. Zenkuda allowed over half of patients to receive injections only once every six months, compared to every eight weeks for Eylea. The company plans to file for FDA approval of Zenkuda in the fourth quarter of 2026.
Key points
- Kodiak Sciences shares rose from $32.35 to $89.92, a 178% gain, adding over $3 billion to market value.
- Zenkuda and tabirafusp-ted were non-inferior to Eylea in visual acuity and retinal drying in the Daybreak trial.
- An AI-guided dosing strategy allowed 54% of Zenkuda patients to extend injection intervals to six months.
- Kodiak plans to file for FDA approval of Zenkuda for wet AMD, diabetic retinopathy, and retinal vein occlusion in Q4 2026.
- Tabirafusp-ted, a bispecific therapy, also matched Eylea, with an FDA filing expected late next year.
Background
This follows a 2023 failure of Zenkuda due to cataract concerns, which was later resolved. The broader eye drug market has seen a shift toward longer dosing intervals, with Roche’s Vabysmo and Regeneron’s Eylea HD already offering 16-20 week intervals. Kodiak’s success challenges these incumbents by offering even longer intervals for a majority of patients.
How outlets are covering it
BioPharma Dive emphasizes the market value surge and the turnaround from a prior trial failure. Fierce Biotech highlights the competitive landscape, noting that Eylea patents have expired, leading to biosimilar competition from Biocon’s Yesafili, and branded rivals like Eylea HD and Vabysmo. Yahoo Finance focuses on the stock price surge, reporting a 178% increase, while BioPharma Dive notes a 128% jump at market open, reflecting different trading moments.
Why it matters
This success could disrupt the dominant eye drug market by offering a more convenient dosing schedule, potentially reducing the burden on ophthalmologists and patients. It also validates Kodiak’s AI-guided dosing strategy, which could influence future trial designs in ophthalmology.
What to watch
Kodiak will file for FDA approval of Zenkuda in Q4 2026 and tabirafusp-ted late next year. The company will also conduct post-hoc analyses to identify patient subgroups that benefit most from IL-6 inhibition with tabirafusp-ted.
- Kodiak skyrockets on positive study data for 2 eye drugs BioPharma Dive
- Kodiak Sciences Up 150% At Opening Bell After Drugs Pass Key Trial Forbes
- Kodiak's stock doubles as resurrected eye disease drug matches Eylea in phase 3 fiercebiotech.com
- Kodiak Sciences soars as Zenkuda, tabirafusp-ted hit primary endpoints in phase III wet AMD trial Yahoo Finance
- Why This Regeneron Eye Rival Just Catapulted More Than 120% Investor's Business Daily
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