Open Label Controlled Trial of Eculizumab in Adolescent Patients With Plasma Therapy-Sensitive aHUS

PHASE2CompletedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

July 31, 2009

Primary Completion Date

October 31, 2010

Study Completion Date

December 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 (13)

14186

Stockholm

16147

Genova

30625

Hanover

33076

Bordeaux

44093

Nantes

67091

Starsbourg

69437

Lyon

75743

Paris

76230

Bois-Guillaume

Unknown

Toronto

Nijmegen

Exeter

Glasgow

Sponsors
All Listed Sponsors
lead

Alexion Pharmaceuticals, Inc.

INDUSTRY