An Efficacy and Safety Study of Ravulizumab in Adult Participants With NMOSD

PHASE3CompletedINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

December 9, 2019

Primary Completion Date

March 15, 2022

Study Completion Date

October 31, 2024

Conditions
Neuromyelitis OpticaNeuromyelitis Optica Spectrum Disorder
Interventions
BIOLOGICAL

Ravulizumab

Participants will receive a weight-based loading dose of ravulizumab via IV infusion on Day 1, followed by weight-based maintenance doses on Day 15, then once every 8 weeks until end of the Long-Term Extension Period.

Trial Locations (41)

1090

Research Site, Vienna

2050

Research Site, Camperdown

3065

Research Site, Fitzroy

8200

Research Site, Aarhus

10117

Research Site, Berlin

10408

Research Site, Goyang-si

20007

Research Site, Washington D.C.

21013

Research Site, Gallarate

28040

Research Site, Madrid

29010

Research Site, Málaga

33136

Research Site, Miami

39216

Research Site, Jackson

45219

Research Site, Cincinnati

55905

Research Site, Rochester

63110

Research Site, St Louis

67098

Research Site, Strasbourg

77030

Research Site, Houston

80045

Research Site, Aurora

80131

Research Site, Napoli

80528

Research Site, Fort Collins

81675

Research Site, München

90015

Research Site, Cefalù

02114

Research Site, Boston

V5G 2X6

Research Site, Burnaby

04103

Research Site, Leipzig

00133

Research Site, Roma

00178

Research Site, Rome

260-0877

Research Site, Chiba

812-8582

Research Site, Fukuoka

350-8550

Research Site, Kawagoe-shi

951-8585

Research Site, Niigata

980-8574

Research Site, Sendai

983-8512

Research Site, Sendai

40-571

Research Site, Katowice

90-324

Research Site, Lódz

02841

Research Site, Seoul

03722

Research Site, Seoul

06351

Research Site, Seoul

143-729

Research Site, Seoul

08036

Research Site, Barcelona

OX3 9DU

Research Site, Oxford

Sponsors
All Listed Sponsors
lead

Alexion Pharmaceuticals, Inc.

INDUSTRY