Corporate presentation
Logotype for Equillium Inc

Equillium (EQ) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Equillium Inc

Corporate presentation summary

27 Oct, 2026

Pipeline and development

  • Wholly owned pipeline targets serious autoimmune and inflammatory disorders: EQ504, an oral colon-targeted AhR modulator for ulcerative colitis; EQ302, an IL-15/21 inhibitor for celiac disease; and an inhaled candidate for lung diseases.

  • EQ504 Phase 1 initiated, with topline data expected Q2 2027; IND-enabling development is underway for the other listed programs.

  • EQ504 is positioned as a selective, tissue-targeted, non-immunosuppressive therapy, with potential formulations for gastrointestinal, lung and skin indications.

EQ504 rationale and ulcerative colitis opportunity

  • EQ504 showed 0.203 nM AhR assay potency, versus 10.39 nM for indirubin, 45.21 nM for tapinarof and 461.8 nM for ITE.

  • Preclinical findings include modulation of Treg, Th17 and macrophage activity; protection of intestinal barrier function and wound healing; and activity in DSS- and TNBS-induced colitis models.

  • A colon-targeted, once-daily oral formulation is designed to deliver drug-coated pellets throughout the colon and maximize tissue exposure while limiting systemic exposure.

  • ~800,000 U.S. patients were treated for UC in 2023; the global market is projected to exceed $12B by 2030, while clinical remission rates remain below ~30% despite 15+ approved therapies.

  • Indigo naturalis studies reported clinical remission up to 50% in controlled Phase 2 studies and up to 27% in treatment-refractory patients; EQ504 is being developed as a controlled, selective alternative to the botanical.

Clinical plan and catalysts

  • EQ504 Phase 1 is a randomized, double-blind, placebo-controlled SAD/MAD study in ~70 healthy volunteers, with five SAD cohorts at 0.1–3.0 mg QD and three MAD cohorts receiving 10 days of daily dosing.

  • Primary endpoint is safety and tolerability; secondary endpoints include blood PK and tissue PK/PD, with multiple colonic biopsies in MAD cohorts.

  • The Phase 1 proof-of-mechanism study was initiated Q4 2026, with topline data expected Q2 2027.

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