14
Participants
Start Date
June 30, 2008
Primary Completion Date
April 30, 2010
Study Completion Date
April 30, 2010
Mangafodipir
"Treatment will be undertaken with a ready-to-use investigative drug formulation identical to what is in diagnostic use as a contrast medium for MRI.~Formulation content: MnDPDP 10 mmol/ml~Administered dose per cycle: 2 μmol/kg b.w. Administration form: Ready-to-use formulation (solution). Mangafodipir or placebo (0.2 ml/kg b.w.) will be administered as an i.v. infusion over 5 min about 30 min prior to start of chemotherapy."
Placebo treatment (0.9% NaCl)
Intravenous infusion, 2 micromol/kg, pretreatment 30 minutes before the start of FOLFOX treatment (during the first three FOLFOX treatments)
Onkologkliniken, Länssjukhuset Ryhov, Jönköping
Lead Sponsor
Egetis Therapeutics
INDUSTRY