drugset / Trial / NCT02546284

Study of Lenzilumab in Previously Treated Patients With Chronic Myelomonocytic Leukemia (CMML)

NCT02546284

Phase 1 Completed 15 enrolled Humanigen, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, repeat-dose, Phase 1 Dose Escalation Study to evaluate safety, pharmacokinetics, and clinical activity.

Timeline

Start
2016-07
Primary completion
2020-02
Completion
2020-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenzilumab Monoclonal antibody 200 mg Intravenous
Subject Lenzilumab Monoclonal antibody 400 mg Intravenous
Subject Lenzilumab Monoclonal antibody 600 mg Intravenous