Excellergy Raises $70M to Rewrite the Allergy Playbook with Trifunctional Biologics

A new force has entered the allergy‑therapeutics arena. Excellergy has announced a bold $70 million Series A round designed to advance its lead candidates—“trifunctional” Effector Cell Response Inhibitors (ECRIs)—toward clinical proof. The molecules aim to simultaneously strip IgE from bound immune cells, neutralize free IgE, and tamp down the receptor expression that fuels allergic cascades.

From its 2021 genesis, seeded by Red Tree Venture Capital, Excellergy has built a platform rooted in insights from Stanford and the University of Bern around how IgE binds its high-affinity receptor FceRI. The company’s pipeline extends this foundational biology into differentiated therapeutics that could challenge conventional anti-IgE drugs. Its ambition: reposition the standard of care in asthma, eczema, allergic rhinitis, and other IgE‑driven conditions.

Veteran biotech executive Todd Zavodnick leads as CEO. Speaking of Excellergy’s mission, he states:

“We are not here to refine the status quo. We are here to build a portfolio of category‑defining assets that will advance and reset the standard of care in allergy.”

Zavodnick emphasizes the trifunctional mechanism as more than incremental:

“By directly removing IgE bound to the receptor, our first-in-class trifunctional ECRIs are engineered to shut down the allergic response at its source, something current therapies cannot achieve.”

Alongside him, co-founder and Chief Scientific Officer Geoffrey Harris, DVM, PhD, and Chief Medical Officer Philip Brown, MD, JD, oversee translation of the science into a robust clinical pipeline.

Backing the round is Red Tree Venture Capital, whose founder & managing partner Heath Lukatch, PhD, remarks:

“Excellergy’s potential is extraordinary. By leveraging well-understood IgE biology in a novel way, the company is both differentiated and advancing innovation from a pathway clinicians already trust.”

With this infusion, Excellergy plans to deepen preclinical validation, scale manufacturing, and prepare its lead asset for a Phase 1 study targeted for early 2026. Key steps ahead include toxicology studies, biomarker development, and establishing early human safety — all underpinned by a platform that promises modular adaptation across allergic disease indications.


Editorial View: Why Excellergy Could Shift the Allergy Therapeutics Landscape

Despite decades of research in allergy and immunology, the IgE axis remains stubbornly under‑exploited. Many biologics today aim to mop up free IgE, but few intervene at the receptor or cell-bound level. Excellergy’s trifunctional design is audacious precisely because it attacks all three levers—the bound IgE, the circulating IgE, and the receptor expression itself. If safety and efficacy can align, this could be a generational leap, not just another molecule in a crowded field.

The company is making smart moves on two fronts: platform modularity and therapeutic breadth. By building a “pipeline-in-a-product” structure—i.e. using the same molecular architecture calibrated for different tissue compartments or disease endotypes—Excellergy can expand indication reach without reinventing entirely novel scaffolds each time. It’s a more capital-efficient play for internally scaling innovation across asthma, food allergies, and chronic urticaria.

From an industry vantage, this round also signals something deeper: investor conviction that the next wave in immunology is not just in checkpoint inhibitors or autoimmune suppression, but in finely tuned, tissue‑aware, receptor-level interventions. The presence of Red Tree and its leadership, who have repeatedly backed transformative biotech plays, adds to the credibility.

Risks loom large — translating trifunctional biology into tolerable safety windows in humans is notoriously hard. But the strategic backbone is strong: a credible founding team, clear mechanistic differentiation, and timing in an immune‑driven disease space starved for innovation. If Excellergy executes well, it could become a blueprint for next-gen immunotherapies.

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