Rehabilitation Study in MS Patients

PHASE4TerminatedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

September 30, 2009

Study Completion Date

September 30, 2009

Conditions
Multiple Sclerosis, Relapsing-Remitting
Interventions
DRUG

Interferon beta-1b, FRP within 15 days after randomization

Treatment by Interferon beta-1b (Betaseron, BAY86-5046) for 3 month and beginning of the Functional Rehabilitation Program starting within 6 weeks after randomization

DRUG

Interferon beta-1b, FRP about 6 weeks after randomization

Treatment by Interferon beta-1b (Betaseron, BAY86-5046) for 3 month and beginning of the Functional Rehabilitation Program about 6 weeks after randomization.

Trial Locations (10)

29000

Quimper

30029

Nîmes

31059

Toulouse

34295

Montpellier

35038

Rennes

51091

Reims

59037

Lille

59160

Lomme

68051

Mulhouse

84025

Avignon

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY

NCT00780455 - Rehabilitation Study in MS Patients | Biotech Hunter | Biotech Hunter