Multiple Sclerosis Clinical Trial
A Randomized Controlled Trial of Eculizumab in AQP4 Antibody-positive Participants With NMO (PREVENT Study)
Summary
The objectives of this time-to-event study were to assess the efficacy and safety of eculizumab as compared with placebo in participants with neuromyelitis optica spectrum disorder (NMOSD) who were anti-aquaporin-4 (AQP4) antibody-positive.
Eligibility Criteria
Key Inclusion Criteria:
Male or female participants ≥ 18 years old.
Diagnosis of NMO or NMOSD.
AQP4 antibody seropositive.
Historical relapse of at least 2 relapses in the last 12 months or 3 relapses in the last 24 months with at least 1 relapse in the 12 months prior to the screening.
Expanded Disability Status Scale score ≤ 7.
If a participant entered the study receiving immunosuppressive therapy (IST) for relapse prevention, the participant must have been on a stable maintenance dose of IST(s), as defined by the treating physician, prior to Screening and must have remained on that dose for the duration of the study, unless the participant experienced a relapse.
Female participants of childbearing potential were to have a negative pregnancy test (serum human chorionic gonadotropin). Participants were required to practice an effective, reliable, and medically approved contraceptive regimen during the study and for up to 5 months following discontinuation of treatment.
Key Exclusion Criteria:
Use of rituximab within 3 months prior to Screening.
Use of mitoxantrone within 3 months prior to Screening.
Use of intravenous immunoglobulin within 3 weeks prior to Screening.
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There are 69 Locations for this study
Scottsdale Arizona, 85259, United States
Carlsbad California, 92011, United States
Washington District of Columbia, 20007, United States
Miami Florida, 33136, United States
Orlando Florida, 32806, United States
Fort Wayne Indiana, 46804, United States
Kansas City Kansas, 66160, United States
Lexington Kentucky, 40503, United States
Baltimore Maryland, 21201, United States
Baltimore Maryland, 21287, United States
Rochester Minnesota, 55905, United States
Saint Louis Missouri, 63110, United States
New York New York, 10016, United States
Gahanna Ohio, 43230, United States
Philadelphia Pennsylvania, 19104, United States
Pittsburgh Pennsylvania, 15213, United States
Dallas Texas, 75246, United States
Salt Lake City Utah, 84132, United States
Seattle Washington, 98122, United States
Ciudad Autonoma, Buenos Aires Buenos Aires, 1425, Argentina
Ciudad Autonoma, Buenos Aires Buenos Aires, C1221, Argentina
Pilar Buenos Aires, B1629, Argentina
Rosario Santa Fe, S2000, Argentina
Camperdown New South Wales, 2050, Australia
Fitzroy Victoria, 3065, Australia
Zagreb , 10000, Croatia
Praha , 128 2, Czechia
Ã…rhus , 8000, Denmark
Heidelberg Baden Wuerttemberg, 69120, Germany
Munich Bayern, 81675, Germany
Rostock , 18147, Germany
Shatin , , Hong Kong
Catania , 95123, Italy
Napoli , 80131, Italy
Rome , 00151, Italy
Rome , 00178, Italy
Chiba-shi Chiba, 260-8, Japan
Nishinomiya-shi Hyogo, 663-8, Japan
Kyoto-shi Kyoto, 604-8, Japan
Sendai-shi Miyagi, 980-8, Japan
Bunkyo-ku Tokyo, 113-8, Japan
Ube-shi Yamaguchi, 755-8, Japan
Fukuoka , 812-8, Japan
Tokio , 187-8, Japan
Goyang-si Gyeonggi-do, 10408, Korea, Republic of
Seoul , 02841, Korea, Republic of
Seoul , 03080, Korea, Republic of
Seoul , 03722, Korea, Republic of
Seoul , 06351, Korea, Republic of
Kuala Lumpur , 50586, Malaysia
Kazan , 42002, Russian Federation
Krasnoyarsk , 63003, Russian Federation
Novosibirsk , 63006, Russian Federation
Rostov-on Don , 34402, Russian Federation
St. Petersburg , 19702, Russian Federation
Barakaldo Bizkaia, 48903, Spain
Cordoba , 14011, Spain
Madrid , 28040, Spain
Taipei , 112, Taiwan
Dusit , 10300, Thailand
Pathumthani , 12120, Thailand
Ubon Ratchathani , 34000, Thailand
Ankara , 06100, Turkey
Istanbul , 34098, Turkey
Istanbul , 34381, Turkey
Izmir , 35340, Turkey
Kocaeli , 41380, Turkey
Samsun , 55139, Turkey
Liverpool , L9 7L, United Kingdom
Oxford , OX3 9, United Kingdom
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