Transition to Rebif New Formulation

PHASE3CompletedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

April 30, 2008

Study Completion Date

April 30, 2008

Conditions
Relapsing Multiple Sclerosis
Interventions
DRUG

Rebif New Formulation + prophylactic Ibuprofen

Subjects, currently on Rebif® 44 mcg three times a week, using Rebiject II as an injection device and having received Rebif® full dose 44 mcg three times a week for at least 6 months, receives systematically 400 mg ibuprofen as prophylactic treatment against flu-like symptoms on days when Rebif New Formulation 44 mcg three times a week is injected

DRUG

Rebif New Formulation + ibuprofen PRN

Subjects, currently on Rebif® 44 mcg three times a week, using Rebiject II as an injection device and having received Rebif® full dose 44 mcg three times a week for at least 6 months, should not administer Ibuprofen before the first Rebif New Formulation injection. If flu-like symptoms occur after the 44 mcg Rebif New Formulation injection then the subject can administer 400 mg ibuprofen. This should only be administered after the Rebif New Formulation injection and not before the Rebif New Formulation injection.

Trial Locations (2)

Unknown

Local Medical Information, Paris

Local Medical Information, Munich

All Listed Sponsors
lead

Merck KGaA, Darmstadt, Germany

INDUSTRY

NCT00619307 - Transition to Rebif New Formulation | Biotech Hunter | Biotech Hunter