drugset / Trial / NCT00574288

Daratumumab (HuMax®-CD38) Safety Study in Multiple Myeloma

NCT00574288 ↗

Phase 2 Completed 104 enrolled Janssen Research & Development, LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Establishment of safety profile of HuMax-CD38 when given as monotherapy in participants with multiple myeloma relapsed from or refractory to at least 2 different cytoreductive therapies and without further established treatment options.

Timeline

Start
2008-03-26
Primary completion
2015-01-09
Completion
2017-04-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Daratumumab Monoclonal antibody 0.005 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 8 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 24 mg/kg Intravenous

Indications