Kodiak Sciences Eye Drug Meets Main Goal in Late Stage Study

Kodiak Sciences shares rose 52 percent after its drug Zenkuda met trial goals for eye damage. The firm plans to accelerate its application for FDA approval.

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Shares of Kodiak Sciences Inc. jumped 52% before the market opened on Thursday following news that its experimental drug, Zenkuda, achieved its primary goal in a late-stage study. The trial focused on patients with diabetic retinopathy, a condition caused by damage to the blood vessels in the retina that can result in significant vision loss. In the clinical trial, 62.5% of patients treated with Zenkuda saw at least a two-step improvement on a standard retinopathy severity scale after 48 weeks. This stands in sharp contrast to the 3.3% improvement observed in the sham treatment group. Additionally, the drug was linked to an 85% lower risk of developing severe complications, such as proliferative diabetic retinopathy. In a statement regarding the clinical findings, the company noted: > Zenkuda was well tolerated, with the study reporting no cases of vision-threatening conditions such as inflammation of blood vessels or the eye. Zenkuda is designed as a long-acting treatment that inhibits a protein responsible for the growth of abnormal blood vessels in the eye. The company observed consistent results across patient groups, including those using GLP-1 medications. Following the successful trial, the developer intends to expedite its application for approval with the Food and Drug Administration in the United States.

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