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OncoMatch/Clinical Trials/NCT06624085

A Study Evaluating the Safety and Efficacy of Glofitamab + Gemcitabine + Oxaliplatin in U.S. Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Is NCT06624085 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments for lymphoma.

Phase 1RecruitingHoffmann-La RocheNCT06624085Data as of Jun 2026

Treatment: Glofitamab · Tocilizumab · Obinutuzumab · Gemcitabine · OxaliplatinThe purpose of the study is to evaluate glofitamab + gemcitabine + oxaliplatin in participants in the United States, including under-represented racial and ethnic populations, that have relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL).

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Extracted eligibility criteria

Treatments studied

Immunotherapy

GlofitamabObinutuzumab

Chemotherapy

GemcitabineOxaliplatin

Other

Tocilizumab

Cancer type

Non-Hodgkin Lymphoma

Hodgkin Lymphoma

Performance status

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

Prior therapy

Min 1 prior line

Must have received: systemic therapy

At least one prior line of systemic therapy

Cannot have received: glofitamab or other bispecific antibodies targeting both CD20 and CD3

Prior treatment with glofitamab or other bispecific antibodies targeting both CD20 and CD3

Cannot have received: gemcitabine (gemcitabine)

Prior treatment with gemcitabine

Cannot have received: oxaliplatin (oxaliplatin)

Prior treatment with oxaliplatin

Cannot have received: monoclonal antibody

Exception: within 4 weeks prior to first study treatment

Treatment with monoclonal antibodies for the purposes of treating cancer within 4 weeks prior to first study treatment

Cannot have received: radiotherapy, chemotherapy, immunotherapy, immunosuppressive therapy, or any investigational agent

Exception: within 2 weeks prior to first study treatment

Treatment with radiotherapy, chemotherapy, immunotherapy, immunosuppressive therapy, or any investigational agent for the purposes of treating cancer within 2 weeks prior to first study treatment

Cannot have received: systemic immunosuppressive medications

Exception: within 4 weeks prior to first dose of study treatment

Prior treatment with systemic immunosuppressive medications within 4 weeks prior to first dose of study treatment

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

US trial sites

  • UC San Diego Moores Cancer Center · La Jolla, California
  • Saddleback Memorial Medical Center · Laguna Hills, California
  • University of California Los Angeles (UCLA) - Cancer Care - Santa Monica · Santa Monica, California
  • Georgetown University · Washington D.C., District of Columbia
  • AdventHealth Cancer Institute · Orlando, Florida

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06624085 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior glofitamab or other bispecific antibodies targeting both CD20 and CD3, gemcitabine, oxaliplatin 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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