An Efficacy and Safety Study of Intetumumab (CNTO 95) in Participants With Metastatic Hormone Refractory Prostate Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

131

Participants

Timeline

Start Date

May 31, 2007

Primary Completion Date

November 30, 2009

Study Completion Date

November 30, 2009

Conditions
Prostatic Neoplasms
Interventions
DRUG

Docetaxel

Docetaxel 75 mg/m\^2 as intravenous infusion every 3 weeks.

DRUG

Prednisone

Prednisone 5 mg orally twice daily.

BIOLOGICAL

Intetumumab

Intetumumab 10 mg/kg as intravenous infusion every week for initial 6 weeks, then every 3 weeks.

DRUG

Placebo

Placebo matching to intetumumab, as intravenous infusion every week for initial 6 weeks, then every 3 weeks.

Trial Locations (59)

Unknown

Birmingham

Los Angeles

San Bernardino

Wichita

Shreveport

Charleston

North Charleston

Graz

Vienna

Wels

Antwerp

Brasschaat

Brussels

Haine-Saint-Paul, La Louviere

Leuven

Liÿge

Ottignies

Roeselare

Tournai

Wilrijk

Aschaffenburg

Berlin

Cologne

Freiburg im Breisgau

Kirchheim

Marburg

München

Tübingen

Ahmedabad

Bangalore

Chennai

Mumbai

New Delhi

Pune

Apeldoorn

Leiden

Maastricht

Nijmegen

The Hague

Bydgoszcz

Gdansk

Inowrocław

Kościerzyna

Lodz

Lublin

Moscow

Moscow Region

Saint Petersburg

St-Petersburg Leningrad

Voronezh

Yaroslavl

Yekaterinburg

Johannesburg Gauteng

Pretoria

Pretoria Gauteng

Cambridge

Leicester

Lincoln

London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Centocor, Inc.

INDUSTRY

NCT00537381 - An Efficacy and Safety Study of Intetumumab (CNTO 95) in Participants With Metastatic Hormone Refractory Prostate Cancer | Biotech Hunter | Biotech Hunter