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

PHASE2TerminatedINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

November 30, 2008

Study Completion Date

November 30, 2008

Conditions
Cancer, Prostate
Interventions
DRUG

Mitoxantrone

Mitoxantrone 12 mg/m\^2 intravenously as a 30 minute infusion on Day 1 of each 3-week cycle until disease progression or unacceptable toxicity or up to 10 cycles (a maximum cumulative dose of approximately 120 mg/m\^2)

DRUG

Siltuximab

Siltuximab 6 mg/kg intravenously as a 2 hour infusion every 2 weeks until disease progression or unacceptable toxicity or up to a maximum of 1 year

DRUG

Prednisone

Prednisone 5 mg orally twice daily

Trial Locations (34)

Unknown

Norwalk

Port Saint Lucie

Atlanta

Shreveport

Baltimore

St Louis

New York

Philadelphia

Charleston

North Charleston

Milwaukee

Innsbruck

Sankt Veit an der Glan

Vienna

Wels

Aalst

Antwerp

Brasschaat

Brussels

Roeselare

Sint-Niklaas

Wilrijk

Caen

Le Mans

Lyon

Villejuif

Berlin

Cologne

Kassel

Barcelona

Madrid

Málaga

London

Sutton

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Centocor, Inc.

INDUSTRY