Exonate

Exonate

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Private Company

Total funding raised: $28.2M

Overview

Exonate is a clinical-stage biotech pioneering a first-in-class, topical therapy for retinal vascular diseases. Its lead asset, EXN407, is a small molecule SRPK1 inhibitor designed as an eye drop to treat diabetic retinopathy and diabetic macular oedema by influencing VEGF alternative splicing. Having completed a Phase Ib/IIa trial, the company is preparing for a Phase IIb trial in 2026, positioning itself to address a significant unmet need for non-invasive treatments. Founded in 2013 as a university spin-out, Exonate is a private, well-funded company with strong scientific foundations and advisory support.

OphthalmologyRetinal Vascular Diseases

Technology Platform

Proprietary small molecule inhibitors of SRPK1, a kinase that regulates VEGF alternative splicing. The platform aims to shift VEGF production from pro-angiogenic to anti-angiogenic isoforms, enabling development of topical eye drop therapies for retinal diseases.

Funding History

2
Total raised:$28.2M
Series A$25M
Seed$3.2M

Opportunities

The primary opportunity is to become the first company to market a topical eye drop for diabetic retinopathy and diabetic macular oedema, addressing a massive unmet need for early, non-invasive treatment.
Success here would also validate the platform for the even larger wet AMD market, potentially disrupting the standard of care dominated by intravitreal injections.

Risk Factors

The key risks are clinical failure of the novel SRPK1 mechanism in late-stage trials, the significant challenge of achieving retinal bioavailability with a topical formulation, and intense competition from established injectable therapies and other novel delivery technologies.
The company also faces financial risk as a private entity dependent on future fundraising.

Competitive Landscape

Exonate competes in the retinal disease market dominated by anti-VEGF injectables (e.g., Roche/Genentech, Regeneron, Bayer). Its primary differentiation is the topical route of administration. Competition also comes from companies developing longer-acting injections, implants, and gene therapies to reduce treatment burden. Its novel splicing mechanism is a unique scientific approach.