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OncoMatch/Clinical Trials/NCT04669171

A Novel Vaccine (EO2463) as Monotherapy and in Combination, for Treatment of Patients With Indolent Non-Hodgkin Lymphoma

Is NCT04669171 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including EO2463 and rituximab for follicular lymphoma.

Phase 1/2RecruitingEnteromeNCT04669171Data as of Jun 2026Location: International · 4 countries

Treatment: EO2463 · lenalidomide · rituximabThe purpose of this study is to define the recommended Phase 2 Dose, safety, tolerability, immunogenicity, and preliminary efficacy of EO2463 during monotherapy and in combination with lenalidomide and/or rituximab in patients with indolent NHL

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Extracted eligibility criteria

Treatments studied

Immunotherapy

rituximab

Endocrine / hormonal

lenalidomide

Other

EO2463

Cancer type

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: any systemic therapy

have received at least one prior line of treatment

Cannot have received: EO2463 (EO2463)

prior exposure to EO2463

Cannot have received: immunotherapy (immunostimulatory or immunosuppressive therapy)

immunotherapy (meaning immunostimulatory or immunosuppressive therapy; beside excluded, or allowed, compounds per other inclusion/exclusion criteria specifications)

Cannot have received: radionuclide therapy

radionuclide therapy

Cannot have received: radiotherapy

Exception: radiotherapy as only prior treatment is allowed in newly diagnosed, previously untreated cohorts

radiotherapy

Cannot have received: cytoreductive therapy

cytoreductive therapy

Cannot have received: investigational agent

treatment with any other investigational agent within 28 days before the first EO2463 administration

Cannot have received: rituximab or other B cell ablation therapy

received rituximab or other B cell ablation therapy within 8 weeks of start of study treatment

Cannot have received: CAR T-cell therapy

Exception: exclusion only if progressed within 6 months after this therapy

received prior CAR T-cell therapy and progressed within 6 months after this therapy

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Dana Farber Cancer Institute · Boston, Massachusetts
  • Mayo Clinic · Rochester, Minnesota
  • University of Rochester Medical Center (URMC) - Wilmot Cancer Institute (WCI) (James P. Wilmot Cancer Center) · Rochester, New York
  • University of Washington-Seattle Cancer Care Alliance · Seattle, Washington

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT04669171 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior EO2463, immunotherapy (immunostimulatory or immunosuppressive therapy), radionuclide therapy disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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