Kodiak Sciences stock triples as Zenkuda matches Eylea in Phase 3 trial

Kodiak Sciences shares surged nearly 178% after its Phase 3 Daybreak trial results showed that both Zenkuda and tabirafusp-ted matched the efficacy of aflibercept (Eylea) for wet age-related macular degeneration. The company plans to file for FDA approval of Zenkuda in the fourth quarter of 2026, citing data that allows for extended dosing intervals.
Key points
- Kodiak Sciences stock jumped from $32.35 to $89.92, a 178% increase, following the release of Phase 3 trial data.
- The Daybreak trial compared Zenkuda (tarcocimab) and tabirafusp-ted to aflibercept, finding both candidates met the primary endpoint for vision gains.
- Zenkuda enabled over half of patients to maintain 24-week dosing intervals, compared to the standard eight-week schedule for aflibercept.
- The company intends to submit a multi-indication FDA application for Zenkuda in Q4 2026, including data from five Phase 3 trials.
- Tabirafusp-ted, a bispecific therapy, also matched aflibercept, though detailed comparative data remains pending post-hoc analysis.
Background
Kodiak Sciences previously halted Zenkuda development in 2023 due to an unexpected increase in cataracts but resumed trials later that year based on diabetic retinopathy data. This recent success marks a significant turnaround for the company, moving it closer to commercialization after previous setbacks.
How outlets are covering it
Fierce Biotech highlights the competitive landscape, noting that while the results are strong, Kodiak faces challenges from biosimilars and branded rivals like Eylea HD and Vabysmo. Yahoo Finance focuses primarily on the dramatic stock market reaction, emphasizing the 178% surge and the specific price points, whereas Fierce Biotech provides clinical context regarding the AI-guided dosing algorithm and safety profiles.
Why it matters
The success of Zenkuda could disrupt the market for anti-VEGF therapies by offering a treatment with significantly longer dosing intervals, potentially reducing the burden on patients and healthcare systems. A successful FDA filing would establish Kodiak as a major player in the ophthalmology sector.
What to watch
Kodiak Sciences will file for FDA approval of Zenkuda in the fourth quarter of 2026. The company will also conduct post-hoc analyses to identify patient subgroups that benefit most from tabirafusp-ted and continue Phase 3 trials for diabetic macular edema.
- Kodiak Sciences soars as Zenkuda, tabirafusp-ted hit primary endpoints in phase III wet AMD trial Yahoo Finance
- 🔎 Under the Radar: Kodiak Stock Surges as Eye Drug Matches Regeneron’s WSJ
- Kodiak Sciences Up 150% At Opening Bell After Drugs Pass Key Trial Forbes
- Why This Regeneron Eye Rival Just Catapulted More Than 170% Investor's Business Daily
- Kodiak's stock doubles as resurrected eye disease drug matches Eylea in phase 3 Fierce Biotech
Want the full story? Read the original reporting
Read on Yahoo Finance