Open Label Controlled Trial of Eculizumab in Adult Patients With Plasma Therapy-Resistant aHUS

PHASE2CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

May 31, 2009

Primary Completion Date

September 30, 2010

Study Completion Date

July 31, 2013

Conditions
Atypical Hemolytic Uremic Syndrome
Interventions
DRUG

Eculizumab

All patients received open-label eculizumab administered intravenously on the following dose schedule: Induction dose - 900 mg per week for four weeks and a dose of 1200 mg one week later; Maintenance dose - 1200 mg every two weeks. Patients who received plasma exchange or infusion during the eculizumab treatment period received a supplemental dose of 600 mg within one hour before plasma infusion or within one hour after the completion of each plasma exchange

Trial Locations (17)

6020

Innsbruck

10032

New York

10065

New York

29107

Quimper

30322

Atlanta

33076

Bordeaux

37044

Tours

42270

Saint-Priest-en-Jarez

44093

Nantes

45147

Essen

46804

Fort Wayne

52074

Aachen

69437

Lyon

75743

Paris

76051

Grapevine

77030

Houston

NE7 7DN

Newcastle

Sponsors
All Listed Sponsors
lead

Alexion Pharmaceuticals, Inc.

INDUSTRY