KOD Stock Up as Jefferies Upgrades Rating on Huge Pipeline Potential

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Shares of Kodiak Sciences KOD rallied 29.6% on Monday after an eminent financial services company, Jefferies, upgraded KOD to a “BUY” rating stating that the company has a major “turnaround story” in place for 2025. Kodiak has lately been garnering immense investor attention driven by the significant potential of its ongoing late-stage studies on the lead candidate, tarcocimab, for retinal disease indications and other pipeline programs.

Tarcocimab, a novel anti-VEGF antibody biopolymer conjugate, is being developed for diabetic eye disease and wet age-related macular degeneration (wet AMD).

In its report, Jefferies stated that at $7 per share ($400 million market cap), the stock price is greatly undervalued and set a target price of $20, translating to a market cap of more than $1 billion in 2025, ahead of phase III data readouts. By 2026, Jefferies projects the stock price to approach $30-$50 or $1.5-$3 billion in market cap.

Let us dig deeper into the catalysts behind Jefferies’ optimism regarding the growth of Kodiak Sciences in the near future.

KOD’s Lead Program Exhibits Significant Potential

In late 2023, Kodiak rebooted the development program of tarcocimab following positive phase III results from the GLOW study, which evaluated the treatment in patients with moderately severe to severe non-proliferative diabetic retinopathy (NPDR).

The company had previously reported the success of its phase III DAYLIGHT and BEACON studies evaluating tarcocimab in patients with wet AMD and retinal vein occlusion (RVO), respectively.The positive data readouts from DAYLIGHT, BEACON and GLOW studies give the company three successful phase III pivotal studies with the candidate across three different retinal vascular and exudative diseases, such as wet AMD, RVO and NPDR.

Leveraging the GLOW1 study's success, Kodiak initiated the GLOW2 study in late 2023 to further investigate tarcocimab for diabetic retinopathy and began dosing patients in May 2024, with enrollment expected to be completed soon. The success of the GLOW2 study is expected to serve as the basis for a single biologics license application submission for tarcocimab, seeking its approval.

The revival of tarcocimab in Kodiak's pipeline, after a major setback earlier in 2023, has restored stakeholder confidence in the candidate’s potential for treating retinal diseases.

In the past three months, shares of KOD have skyrocketed 310.9% against the industry’s 6.3% decline.

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KOD’s Other Pipeline Programs Progressing Well

Kodiak is also developing KSI-501, a dual inhibitor bioconjugate molecule, to address inflammation and abnormal blood vessel growth in retinal vascular diseases.