71
Participants
Start Date
March 31, 2012
Primary Completion Date
January 31, 2013
Study Completion Date
January 31, 2013
RLX030
Intravenous infusion of RLX030 over 20 hrs
Placebo
Intravenous infusion of placebo over 20 hours
Novartis Investigative Site, Berlin
Novartis Investigative Site, Greifswald
Novartis Investigative Site, Brescia
Novartis Investigative Site, Dortmund
Novartis Investigative Site, Bad Nauheim
Novartis Investigative Site, Erfurt
Novartis Investigative Site, Moscow
Novartis Investigative Site, Moscow
Novartis Investigative Site, Saint Petersburg
Novartis Investigative Site, Saint Petersburg
Novartis Investigative Site, S.-Petersburg
Novartis Investigative Site, Saint Petersburg
Novartis Investigative Site, Tomsk
Novartis Investigative Site, Kemerovo
Novartis Investigative Site, Buenos Aires
Novartis Investigative Site, Caba
Novartis Investigative Site, Halle
Novartis Investigative Site, Groningen
Novartis Investigative Site, Warsaw
Novartis Investigative Site, Wroclaw
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY