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

Hoffmann-La Roche
NCT IDNCT06624085ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

50

Study length

about 4.9 years

Ages

18+

Locations

15 sites in CA, DC, FL +8

Why this study is shown

Actively enrollingPHASE1

What this study is about

Researchers are testing a treatment with glofitamab, gemcitabine, and oxaliplatin for people in the United States who have relapsed or refractory diffuse large B-cell lymphoma. The trial will last about 1798 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Gemcitabine
  • 2.Take Glofitamab
  • 3.Take Obinutuzumab
  • +2 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

gemcitabine, glofitamab, obinutuzumab, oxaliplatin, tocilizumab (Monoclonal antibody; blocks IL-6 receptor to reduce inflammation)

Drug routes

injection (Injection), injection, intravenous, infusion

Endpoints

Primary: Complete response (CR) rate, Incidence of Adverse Events (AEs)

Secondary: Duration of CR, Duration of response (DOR), Objective response rate (ORR), Overall Survival (OS), Progression-free survival (PFS)

Body systems

Oncology