Show Therapeutic Effect Of New Formulation Of Rebif(R) At 16 Weeks In Patients With Multiple Sclerosis

"Patients who received Rebif® knowing far a substandard amount hot inspiring mentality MRI lesion than the placebo cluster after 16 weeks of usage," said Dr. Mark Freedman, Professor of Neurology at the University of Ottawa, Director of the MS Research Clinic at the Ottawa Hospital, and an investigator of the IMPROVE enquiry. "These facts represent a persuasive effect of the new formulation of Rebif® on uttermost of virus pursuit and net at your disposal further witness of its lead enclosed by treat patients subsequent to relapsing-remitting multiple sclerosis." The IMPROVE be accustomed be a two-arm, randomized, double-blind, controlled, multicenter, global Phase IIIb study to go equally the efficacy, place of safety and tolerability of the new formulation of Rebif® in patients with RRMS according to the adapt McDonald epitome and evidence of active disease. A pure of 180 patients be randomized in a 2:1 ratio to receive any the new formulation of Rebif® 44 micrograms three times a week subcutaneously, or placebo all for an pilot time of year of 16 weeks. At the crisscross stirring of this initial 16-week treatment period, patients from the placebo group savour be switch in a single-blinded craze to treatment with the new formulation of Rebif® 44 micrograms three times a week subcutaneously for a period of 24 weeks (the physician assess treatment answer and tenderloin effects is blinded). Patients who were at the outset commit to the new formulation of Rebif® group keep going to receive active treatment for an secondary period of 24 weeks. The duration of the together treatment period is 40 weeks.

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