drugset / Trial / NCT02257567

A Study of Polatuzumab Vedotin (DCDS4501A) in Combination With Rituximab or Obinutuzumab Plus Bendamustine in Participants With Relapsed or Refractory Follicular or Diffuse Large B-Cell Lymphoma

NCT02257567 ↗

Phase 1/2 Completed 331 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a multicenter, open-label study of polatuzumab vedotin administered by intravenous (IV) infusion in combination with standard doses of bendamustine (B) and rituximab (R) or obinutuzumab (G) in participants with relapsed or refractory follicular lymphoma (FL) or diffuse large B-cell lymphoma (DLBCL). The study comprises two stages: a Phase Ib safety run-in stage and a Phase II stage. The anticipated time on treatment is 18 weeks for participants with DLBCL and 24 weeks for participants with FL.

Timeline

Start
2014-10-15
Primary completion
2021-10-21
Completion
2021-10-21

Outcome

Sources disagree · no verdict is set; each source's reading is shown below

registry analysis (superiority test); Arm A (Phase II Randomization): Pola+BR in FL vs Arm B (Phase II Randomization): BR in FL; p = 0.5353 reads as mixed primary results NCT02257567 ↗

registry Arm C (Phase II Randomization): Pola+BR in DLBCL vs Arm D (Phase II Randomization): BR in DLBCL; p = 0.0128 reads as mixed primary results NCT02257567 ↗

registry NUMBER Arm C (Phase II Randomization): Pola+BR in DLBCL: 42.5 (27.04 to 59.11) percentage of participants reads as mixed primary results NCT02257567 ↗

registry NUMBER Arm D (Phase II Randomization): BR in DLBCL: 17.5 (7.34 to 32.78) percentage of participants reads as mixed primary results NCT02257567 ↗

release “with 40% achieving a complete response (CR) compared to 18% in the BR arm (primary endpoint, as measured by positron emission tomography (PET);” reads as met primary endpoint roche.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Obinutuzumab Monoclonal antibody 1000 mg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 1.8 mg/kg Intravenous
Background Bendamustine Small molecule 90 mg/m2 Intravenous
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications