Eculizumab in Pediatric and Adult Participants With Atypical Hemolytic Uremic Syndrome (aHUS) in China

PHASE3CompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

July 14, 2023

Primary Completion Date

May 7, 2025

Study Completion Date

May 7, 2025

Conditions
Atypical Hemolytic Uremic
Interventions
DRUG

Eculizumab

Weight-based doses of Eculizumab will be administered intravenously as an induction dose followed by maintenance dose at Day 8, 15, or 29 depending on weight; then every 2 or 3 weeks, depending upon weight.

Trial Locations (6)

100034

Research Site, Beijing

100045

Research Site, Beijing

110016

Research Site, Qingdao

410007

Research Site, Changsha

430030

Research Site, Wuhan

030012

Research Site, Taiyuan

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

lead

Alexion Pharmaceuticals, Inc.

INDUSTRY