drugset / Trial / NCT01985126

An Efficacy and Safety Study of Daratumumab in Patients With Multiple Myeloma Who Have Received at Least 3 Prior Lines of Therapy (Including a Proteasome Inhibitor [PI] and Immunomodulatory Drug [IMiD]) or Are Double Refractory to a PI and an IMiD

NCT01985126

Phase 2 Completed 124 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of 2 daratumumab treatment regimens in participants with multiple myeloma who have received at least 3 prior lines of therapy (including a proteasome inhibitor \[PI\] and immunomodulatory drug \[IMiD\]) or are double refractory to a PI and an IMiD.

Timeline

Start
2013-09-27
Primary completion
2015-01-09
Completion
2017-05-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Daratumumab Monoclonal antibody 8 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Background Acetaminophen Small molecule 650 mg Oral
Background Acetaminophen Small molecule 1000 mg Oral
Background Diphenhydramine Unknown 25 mg Oral
Background Diphenhydramine Unknown 50 mg Oral
Background Methylprednisolone Other / unclassified Intravenous

Indications