A Rollover Study to Evaluate the Long-Term Safety and Efficacy of Ocrelizumab In Patients With Multiple Sclerosis
- Multiple Sclerosis (MS)
Recruiting
- Abington
- Aguascalientes
- Albuquerque
- Almada
- Aosta
- Atlanta
- Banskobystrický kraj
- Barcelona
- Barnaul
- Basel
- Bergen
- Berlin
- Bilbo
- Bonn
- Bordeaux
- Braga
- Bratislava Region
- Brno-Bohunice
- Bron
- București
- Budapest
- Buenos Aires
- Burlington
- Caen
- Calgary
- Charlotte
- Chernihiv
- Chicago
- Chihuahua
- Ciudad de México
- Clermont-Ferrand
- Columbus
- Concord
- Conflans-Sainte-Honorine
- Culiacán Rosales
- Damme
- Detroit
- Dnipro
- Dresden
- Düsseldorf
- Edmonton
- Essen
- Farmington
- Farmington Hills
- Fitzroy
- Frankfurt
- Gatineau
- Gdańsk
- Genova
- Gießen
- Grodno
- Guadalajara
- Havířov
- Hickory
- Hlavní město Praha
- Houston
- Hradec Králové
- Indianapolis
- Innsbruck
- İstanbul
- Jerusalem
- Jihlava
- Jihomoravský kraj
- Kansas City
- Katowice
- Kaunas
- Kharkiv
- Kirov
- Klaipėda
- Kragujevac
- Kraków
- Laguna Hills
- Leipzig
- Lille
- Linz
- Lombardy
- Long Beach
- Longueuil
- Lubbock
- Lublin
- Lugano
- Lviv
- Madrid
- Manouba
- Memphis
- Miami
- Milano
- Minsk
- Monastir
- Monterrey
- Montréal
- Moscow
- Moscow Oblast
- Málaga
- Münster
- Nancy
- Newark
- Newcastle upon Tyne
- Nice
- Niš
- Odesa
- Oklahoma City
- Orlando
- Ottawa
- Pardubice
- Patchogue
- Petah Tikva
- Phoenix
- Pleven
- Portland
- Porto Alegre
- Prien am Chiemsee
- Providence
- Pécs
- Raleigh
- Ramat Gan
- Regensburg
- Riga
- Rio de Janeiro
- Rio Grande do Sul
- Roeselare
- Roma
- Rosario
- Round Rock
- Rīga
- Saint Petersburg
- Saint-Herblain
- Samsun
- San Antonio
- San Francisco
- Santa Catarina
- Santiago de Compostela
- Saransk
- Seattle
- segrate
- Sevilla
- sicilia
- Siemianowice Śląskie
- Smolensk
- Sofia
- St Leonards
- St. Louis
- State of São Paulo
- Stony Brook
- Strasbourg
- Swansea
- Szeged
- Tacoma
- Tallinn
- Tampa
- Tampere
- Tartu
- Teaneck
- Tel Aviv-Yafo
- Teplice
- therapeutica
- Toronto
- Torrette
- Ulm
- Vancouver
- vara_din
- Vero Beach
- Viciebsk
- Vilnius
- Vologda
- Warszawa
- windsor
- Yekaterinburg
- Zagreb
- Žilinský kraj
NCT05269004 2021-005746-15 MN43964
Trial Summary
This is a Phase IIIb, single-arm, multicenter, OLE study. Participants receiving ocrelizumab as an investigational medicinal product (IMP) in a Roche sponsored Parent study who continue to receive ocrelizumab or are in safety follow-up at the time of the closure of their respective Parent study (WA21092, WA21093 or WA25046) are eligible for enrollment in this extension study. Participants who will continue ocrelizumab treatment will receive IMP based on the dosage and administration received at the time of rollover from the Parent study.
A Multicenter, Single-Arm, Open-Label, Extension, Rollover Study To Evaluate The Long-Term Safety And Efficacy Of Ocrelizumab In Patients With Multiple Sclerosis
Eligibility Criteria
- Prior eligibility for and previous participation in 1 of the Roche-sponsored Parent Studies WA21092, WA21093, or WA25046 with the participant either receiving ocrelizumab as an investigational medicinal product (IMP) or being in safety follow-up after treatment discontinuation
- For female participants of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use adequate acceptable contraception during the treatment period and for at least 6 months or longer if the local label is more stringent after the final dose of ocrelizumab, as applicable in the ocrelizumab package leaflet
- Concurrent participation in any clinical trial (other than the Parent study)
- Unable or unwilling to comply with the requirements of the protocol
For the latest version of this information please go to www.forpatients.roche.com