Atacicept in Subjects With Optic Neuritis

PHASE2TerminatedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

June 30, 2008

Primary Completion Date

September 30, 2009

Study Completion Date

January 31, 2011

Conditions
Optic Neuritis
Interventions
DRUG

Atacicept

Atacicept will be administered subcutaneously at a dose of 150 milligram (mg) twice a week for initial 4 weeks as loading dose, followed by 150 mg once a week for subsequent 32 weeks.

DRUG

Placebo matched to atacicept

Placebo matched to atacicept will be administered subcutaneously twice a week for initial 4 weeks, followed by once a week for subsequent 32 weeks.

Trial Locations (28)

Unknown

Research Site, Birmingham

Research Site, Aurora

Research Site, Fairfield

Research Site, Jacksonville

Research Site, East Lansing

Research Site, Philadelphia

Research Site, Houston

Research Site, Burlington

Research Site, Parkville

Research Site, Brussels

Research Site, Vancouver

Research Site, Ottawa

Research Site, Montreal

Research Site, Hradec Králové

Research Site, Olomouc

Research Site, Paris

Research Site, Freiburg im Breisgau

Research Site, Munich

Research Site, Tübingen

Research Site, Würzburg

Research Site, Beirut

Research Site, Dbaïyé

Research Site, Barcelona

Research Site, Seville

Research Site, Valencia

Research Site, Lausanne

Research Site, London

Research Site, Sheffield

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Merck KGaA, Darmstadt, Germany

INDUSTRY

lead

EMD Serono

INDUSTRY

NCT00624468 - Atacicept in Subjects With Optic Neuritis | Biotech Hunter | Biotech Hunter