drugset / Trial / NCT06468943

Polatuzumab Vedotin and Zanubrutinib Plus R-CHP for Patients With Newly Diagnosed Untreated Non-GCB DLBCL

NCT06468943

Phase 2 Enrolling by invitation 20 enrolled The First Affiliated Hospital of Soochow University
NaSingle-groupOpen-labelTreatment

Summary

Aim of this study will evaluate the efficacy and safety of Polatuzumab Vedotin and Zanubrutinib in combination with R-CHP for newly diagnosed untreated Non-GCB DLBCL Patients with extranodal involvement.

Timeline

Start
2023-07-01
Primary completion
2026-05-01
Completion
2028-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Polatuzumab Vedotin Other / unclassified 1.8 mg/kg Intravenous
Subject Zanubrutinib Small molecule 160 mg
Background Cyclophosphamide Other / unclassified 750 mg/m2 Intravenous
Background Doxorubicin Other / unclassified 50 mg/m2 Intravenous
Background Prednisone Other / unclassified 100 mg
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous