drugset / Trial / NCT02730312

PH 1 Study to Evaluate Safety and Tolerability of XmAb14045 in Patients With CD123-expressing Hematologic Malignancies

NCT02730312

Phase 1 Completed 120 enrolled Xencor, Inc. ICON Clinical Research · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety and tolerability of weekly intravenous (IV) administration of XmAb14045 and to determine the maximally tolerated dose (MTD) after the first dose, and then to determine the MTD after second and subsequent infusions.

Timeline

Start
2016-08
Primary completion
2021-09
Completion
2021-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Vibecotamab Monoclonal antibody 1.7 ug/kg Intravenous