drugset / Trial / NCT06176729

Pola-R2 in Newly Diagnosed Non-fit Elderly DLBCL Patients

NCT06176729

NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, single-arm, phase II study, and the purpose of this study is to evaluate the efficacy and safety of Pola-R2 regimen in newly diagnosed elderly diffuse large B cell lymphoma classified into un-fit or frail group by comprehensive geriatric assessment(CGA).

Timeline

Start
2023-10-24
Primary completion
2025-10-24
Completion
2027-10-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg Oral
Subject Polatuzumab Vedotin Other / unclassified 1.8 mg/kg Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous