10
Participants
Start Date
May 31, 2003
Primary Completion Date
November 30, 2011
Study Completion Date
November 30, 2011
Oxaliplatin
The starting dose of oxaliplatin administered via isolated hepatic perfusion will be the safe tolerated dose of intra-arterial infusion and pharmacokinetics from intravenous studies. The dose will be 5 mg/m2 and will be escalated.
UPMC Presbyterian, Pittsburgh
UPMC Cancer Centers, Hillman Cancer Center, Pittsburgh
UPMC Shadyside, Pittsburgh
Collaborators (1)
The Pittsburgh Foundation
OTHER
Sanofi
INDUSTRY
David Bartlett
OTHER