20
Participants
Start Date
December 31, 2009
Primary Completion Date
May 31, 2013
Study Completion Date
July 31, 2013
Mangafodipir
Administered dose: 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 intravenous (iv.) infusion over 2-5 min prior to reopening of occluded coronary artery during PCI
Placebo
Department of Internal Medicine, County Hospital Ryhov, Jönköping
Lead Sponsor
Egetis Therapeutics
INDUSTRY