drugset / Trial / NCT04892446

Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma

NCT04892446

Phase 2 Terminated 36 enrolled Gilead Sciences
Non-randomizedSequentialOpen-labelTreatment

Summary

The goal of this clinical study is to learn more about the safety and dosing of the study drug, magrolimab, in combination with other anticancer therapies in participants with relapsed/refractory multiple myeloma.

Timeline

Start
2021-11-09
Primary completion
2024-04-25
Completion
2024-04-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.3 mg/m2 Subcutaneous
Subject Carfilzomib Other / unclassified 1.3 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 70 mg/m2 Intravenous
Subject Daratumumab Monoclonal antibody 16 mg/kg Subcutaneous
Subject Daratumumab Monoclonal antibody 1800 mg Subcutaneous
Subject Magrolimab Monoclonal antibody Intravenous
Subject Pomalidomide Other / unclassified 4 mg Oral
Background Dexamethasone Small molecule 40 mg Oral

Indications