60
Participants
Start Date
March 31, 2010
Primary Completion Date
May 31, 2010
Study Completion Date
May 31, 2010
mipomersen sodium
200 mg of mipomersen intravenous (IV) (single dose)
mipomersen sodium
200 mg of mipomersen subcutaneous (SC) (single dose)
moxifloxacin hydrochloride (Avelox®)
400 mg of moxifloxacin intravenous (IV) single dose
placebo
placebo intravenous (IV) single dose
placebo
placebo subcutaneous (SC) single dose
PPD Development, LP, Austin
Lead Sponsor
Collaborators (1)
Ionis Pharmaceuticals, Inc.
INDUSTRY
Kastle Therapeutics, LLC
INDUSTRY