drugset / Trial / NCT07231250

Glofitamab Plus Polatuzumab Vedotin and Zuberitamab in Patients With Newly Diagnosed Diffuse Large B-cell Lymphoma

NCT07231250

Phase 2 Not yet recruiting 40 enrolled Li Zhiming
NaSingle-groupOpen-labelTreatment

Summary

This is a multi-center, phase II, prospective study. The main purpose of study is to evaluate the efficacy and safety of Glofitamab plus Polatuzumab vedotin and Zuberitamab in patients with newly diagnosed diffuse large B-cell lymphoma.

Timeline

Start
2026-01-15
Primary completion
2026-09-15
Completion
2028-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified Intravenous
Subject Doxorubicin Other / unclassified Intravenous
Subject Glofitamab Monoclonal antibody 30 mg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 1.8 mg/kg Intravenous
Subject Prednisone Other / unclassified Oral
Subject Zuberitamab Monoclonal antibody 375 mg/m2 Intravenous
Background Obinutuzumab Monoclonal antibody 1000 mg Intravenous