Study of Ravulizumab in Pediatric Participants With HSCT-TMA

PHASE3CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

December 7, 2020

Primary Completion Date

November 26, 2024

Study Completion Date

May 27, 2025

Conditions
Thrombotic Microangiopathy
Interventions
DRUG

Ravulizumab

Weight-based doses of ravulizumab will be administered intravenously as a loading dose regimen followed by maintenance dosing every 4 or 8 weeks, depending upon weight.

OTHER

Best Supportive Care

Participants will receive medications, therapies, and interventions per standard hospital treatment protocols (unless specifically prohibited by the protocol).

Trial Locations (26)

5505

Research Site, Seoul

8950

Research Site, Esplugues de Llobregat

28046

Research Site, Madrid

30322

Research Site, Atlanta

37007

Research Site, Salamanca

53792

Research Site, Madison

60611

Research Site, Chicago

75235

Research Site, Dallas

80045

Research Site, Aurora

84108

Research Site, Salt Lake City

85724

Research Site, Tucson

91096

Research Site, Haifa

91120

Research Site, Jerusalem

97239

Research Site, Portland

4920235

Research Site, Petah Tikva

5265601

Research Site, Ramat Gan

00165

Research Site, Roma

960-1295

Research Site, Fukushima

650-0047

Research Site, Kobe

466-8560

Research Site, Nagoya

534-0021

Research Site, Osaka

03080

Research Site, Seoul

08041

Research Site, Barcelona

B4 6NH

Research Site, Birmingham

BS2 8BJ

Research Site, Bristol

NE1 4LP

Research Site, Newcastle upon Tyne

Sponsors
All Listed Sponsors
lead

Alexion Pharmaceuticals, Inc.

INDUSTRY