drugset / Trial / NCT01998971

A Study of JNJ-54767414 (HuMax CD38) (Anti-CD38 Monoclonal Antibody) in Combination With Backbone Treatments for the Treatment of Patients With Multiple Myeloma

NCT01998971

Phase 1 Completed 240 enrolled Janssen Research & Development, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and dose regimen of daratumumab when administered in combination with various treatment regimens for the treatment of multiple myeloma.

Timeline

Start
2014-02-18
Primary completion
2019-01-31
Completion
2024-01-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Background Acetaminophen Small molecule Oral
Background Bortezomib Small molecule Subcutaneous
Background Carfilzomib Other / unclassified 70 mg/m2 Intravenous
Background Dexamethasone Small molecule 40 mg Intravenous
Background Diphenhydramine Unknown Intravenous
Background Lenalidomide Other / unclassified Oral
Background Melphalan Small molecule Oral
Background Montelukast Other / unclassified Intravenous
Background Pomalidomide Other / unclassified 4 mg Oral
Background Prednisone Other / unclassified Intravenous
Background Thalidomide Other / unclassified Oral

Indications