3
Participants
Start Date
May 31, 2013
Primary Completion Date
August 31, 2014
Study Completion Date
August 31, 2014
Placebo
Placebo to RLX030 as intravenous infusion for 72 hours
RLX030
RLX030 1 mg/mL vials
Novartis Investigative Site, Mobile
Novartis Investigative Site, Louisville
Novartis Investigative Site, Lexington
Novartis Investigative Site, Modena
Novartis Investigative Site, Galveston
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY