16
Participants
Start Date
July 28, 2015
Primary Completion Date
September 1, 2016
Study Completion Date
September 1, 2016
ALXN1210
ALXN1210 was administered by IV infusion over 5 periods, 1 dose per period: Period 1, induction; Periods 2-5, maintenance. Participants received a total of 5 doses of 400 or 800 mg, each administered every 28 days.
Placebo
Placebo was administered by IV infusion over 5 periods, 1 dose per period. Participants received the same volume and infusion rate as specified for each ALXN1210 dose (400 or 800 mg).
Clinical Trial Site, London
Lead Sponsor
Alexion Pharmaceuticals, Inc.
INDUSTRY