Press Releases October 6, 2026 08:00 AM

Odyssey Therapeutics Announces Oral Presentation of Additional Phase 2a Induction Data for OD-001 in Ulcerative Colitis at UEG Week 2026

Odyssey Therapeutics to present new Phase 2a trial data for OD-001 in ulcerative colitis at UEG Week 2026

By Priya Menon
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Odyssey Therapeutics announced that additional results from the induction period of its Phase 2a trial of OD-001, an oral RIPK2 scaffolding inhibitor for moderate to severe ulcerative colitis, will be presented orally at the upcoming UEG Week 2026. The company will also host a conference call to discuss these new data, underscoring progress in their clinical development program targeting autoimmune and inflammatory diseases.

Odyssey Therapeutics Announces Oral Presentation of Additional Phase 2a Induction Data for OD-001 in Ulcerative Colitis at UEG Week 2026
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Key Points

  • Odyssey Therapeutics is advancing OD-001, a first-in-class oral RIPK2 inhibitor, in a Phase 2a trial for moderate to severe ulcerative colitis.
  • New induction period data will be presented at a major gastroenterology conference (UEG Week 2026).
  • The company is focused on developing precision medicines for autoimmune and inflammatory diseases, indicating potential broader impact in this sector.

Company to host conference call and webcast following the presentation on Tuesday, October 20, at 8:00 a.m. EDT

BOSTON, Oct. 06, 2026 (GLOBE NEWSWIRE) -- Odyssey Therapeutics, Inc. (Nasdaq: ODTX) (“Odyssey” or the “Company”), a clinical-stage biopharmaceutical company seeking to transform the standard of care for patients suffering from autoimmune and inflammatory diseases by developing medicines that precisely target disease pathology, today announced that additional results from the OD-001 induction period of its Phase 2a trial in moderate to severe ulcerative colitis will be featured in an oral presentation at United European Gastroenterology (UEG) Week 2026, taking place October 17-20, in Barcelona, Spain.

The oral presentation details are as follows:

Title: Safety and Efficacy of OD-001, a First-in-class Oral RIPK2 Scaffolding Inhibitor, in Patients with Moderately to Severely Active Ulcerative Colitis: Results from a Phase 2a Trial (NCT06850727)
Presenter: Bruce Sands, M.D., M.S., Dr. Burrill B. Crohn Professor of Medicine and Chief, Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai
Presentation Number: OP197
Date and Time: Tuesday, October 20, at 9:00 a.m. CEST / 3:00 a.m. EDT
Room: UEG Forum

Odyssey will host a conference call and webcast on Tuesday, October 20, 2026, at 8:00 a.m. EDT to review additional data from the OD-001 induction period of the Phase 2a trial beyond those presented at UEG Week 2026. A live webcast will be available under “News and Events” in the Investors section of the Company’s website at www.odysseytx.com on the day of the event. A replay will be archived on the Events page for 180 days.

About Odyssey Therapeutics

Odyssey Therapeutics is a clinical-stage biopharmaceutical company seeking to transform the standard of care for patients suffering from autoimmune and inflammatory diseases by developing medicines that are designed to precisely target disease pathology. Since its founding in 2021, Odyssey has built a portfolio of internally discovered and developed medicines with its first program advancing through multiple clinical milestones. Odyssey’s portfolio leverages the scientific expertise of its team of experienced drug hunters and a comprehensive suite of tools to efficiently advance product candidates that the Company believes have the potential to induce deep and durable remission for patients across several inflammatory diseases with unmet need.

For more information, please visit www.odysseytx.com and follow Odyssey on LinkedIn or X.

Contacts

Benjamin Navon
Senior Director, Communications

For investors
[email protected]

For media
[email protected]


Risks

  • Clinical trial results may not meet expectations, impacting future development and commercialization.
  • Regulatory approval and market adoption of OD-001 remain uncertain due to the competitive and complex nature of autoimmune disease treatments.
  • The biopharmaceutical sector is subject to development, funding, and market risks that could affect the company's progress and valuation.

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