19
Participants
Start Date
February 29, 2004
Primary Completion Date
April 30, 2006
Study Completion Date
April 30, 2006
Docetaxel
Participants will receive docetaxel on Day 1 of each 3-week cycle as 60, 75, or 100 mg/m\^2 via IV infusion. Treatment may continue until disease progression, unacceptable toxicity, or consent withdrawal.
RhuMab 2C4
Participants will receive rhuMab 2C4 on Day 1 of each 3-week cycle as 420 mg via IV infusion. For Cycle 1 ony, rhuMab will be administered on Day 2, at least 24 hours after docetaxel and following an initial 840-mg loading dose. Treatment may continue until disease progression, unacceptable toxicity, or consent withdrawal.
Rotterdam
Sutton
Hoffmann-La Roche
INDUSTRY