drugset / Trial / NCT02159365

Study of Safety of Elotuzumab Administered Over Approximately 60 Minutes in Combination With Lenalidomide and Dexamethasone for Newly Diagnosed or Relapsed/Refractory Multiple Myeloma Patients

NCT02159365

Phase 2 Completed 84 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

To explore whether Elotuzumab dose administration over approximately 60 minutes is feasible and safe.

Timeline

Start
2014-03-08
Primary completion
2016-06-30
Completion
2018-07-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Elotuzumab Monoclonal antibody 10 mg/kg Intravenous
Background Dexamethasone Small molecule 40 mg Oral
Background Lenalidomide Other / unclassified 25 mg Oral

Indications