drugset / Trial / NCT01632852

A Study of CSL362 in Patients With CD123+ Acute Myeloid Leukemia Currently in Remission

NCT01632852

Phase 1 Completed 30 enrolled CSL Limited Parexel · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a first in human, prospective, multicenter, nonrandomized, open-label, dose-escalation study to investigate the safety, pharmacokinetics, pharmacodynamics and immunogenicity of repeat doses of CSL362.

Timeline

Start
2012-07
Primary completion
2015-08
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Talacotuzumab Monoclonal antibody 12 mg/kg Intravenous