drugset / Trial / NCT00385827

A Safety and Efficacy Study of Siltuximab (CNTO 328) in Male Subjects With Metastatic Hormone-Refractory Prostate Cancer (HRPC)

NCT00385827

Phase 2 Terminated 106 enrolled Centocor, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and efficacy of siltuximab administered in combination with mitoxantrone and prednisone in participants with metastatic (spread of cancer cells from one part of the body to another) hormone-refractory (not responding to treatment) prostate cancer (abnormal tissue that grows and spreads in the body) (HRPC).

Timeline

Start
2006-11
Primary completion
2008-11
Completion
2008-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Siltuximab Monoclonal antibody 6 mg/kg Intravenous
Background Mitoxantrone Small molecule 12 mg/m2 Intravenous
Background Prednisone Other / unclassified 5 mg Oral

Indications