drugset / Trial / NCT02953509

Trial of Magrolimab (Hu5F9-G4) in Combination With Rituximab or Rituximab + Chemotherapy in Participants With Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma

NCT02953509

Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objectives of this study are: * To investigate the safety and tolerability, and to define the recommended Phase 2 dose and schedule (RP2DS) for magrolimab in combination with rituximab and for magrolimab in combination with rituximab, gemcitabine, and oxaliplatin (R-GemOx). * To evaluate the efficacy of magrolimab in combination with rituximab in participants with indolent lymphoma and diffuse large B-cell lymphoma (DLBCL) and to evaluate the efficacy of magrolimab in combination with R-GemOx in autologous stem cell transplant (ASCT) ineligible DLBCL participants.

Timeline

Start
2016-11-21
Primary completion
2024-03-25
Completion
2024-03-25

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Magrolimab Monoclonal antibody 10 mg/kg Intravenous
Subject Magrolimab Monoclonal antibody 20 mg/kg Intravenous
Subject Magrolimab Monoclonal antibody 30 mg/kg Intravenous
Subject Magrolimab Monoclonal antibody 45 mg/kg Intravenous
Background Allopurinol Small molecule 300 mg Oral
Background Gemcitabine Small molecule 1000 mg/m2 Intravenous
Background Oxaliplatin Small molecule 100 mg/m2 Intravenous
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications