drugset / Trial / NCT04778410

Study of Magrolimab Combinations in Participants With Myeloid Malignancies

NCT04778410

Phase 2 Terminated 54 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 (Mag), in combination with anti-leukemia therapies in participants with acute myeloid leukemia (AML).

Timeline

Start
2021-06-28
Primary completion
2024-03-04
Completion
2024-03-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Magrolimab Monoclonal antibody 30 mg/kg Intravenous
Background Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Background Azacitidine Other / unclassified 300 mg Oral
Background Cytarabine Small molecule 1000 mg/m2 Intravenous
Background Etoposide Small molecule 100 mg/m2 Intravenous
Background Mitoxantrone Small molecule 8 mg/m2 Intravenous
Background Venetoclax Small molecule 400 mg Oral

Indications