drugset / Trial / NCT01309412

A Phase 1 Study of CNTO 328 (Siltuximab) in Relapsed or Refractory Multiple Myeloma

NCT01309412

Phase 1 Terminated 9 enrolled Janssen Pharmaceutical K.K.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and the tolerability of siltuximab up to 11.0 mg/kg in combination with bortezomib and dexamethasone for patients with relapsed or refractory multiple myeloma.

Timeline

Start
2011-01
Primary completion
2012-12
Completion
2012-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Siltuximab Monoclonal antibody 5.5 mg/kg Intravenous
Subject Siltuximab Monoclonal antibody 11 mg/kg Intravenous

Indications