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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 (May 2026). This Phase 1 trial studies multiple treatments for lymphoma.

Phase 1RecruitingHoffmann-La RocheNCT06624085Data as of May 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

Cancer type

Non-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 →

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