Placebo-controlled phase 3 study of oral BG-12 for relapsing MS


Data from this randomised, double-blind, placebo-controlled phase 3 study oral BG-12 in relapsing remitting MS (RRMS) shows a reduction in annualised relapse rate of approximately 50% compared to placebo.

Overall there was also a relative risk reduction for disability progression in treated patients of approximately a third. Using a three-times-a-day dosing regime was no superior to the twice-a-day dosing regimen.

Authors: Gold R, Kappos L, Arnold DL, Bar-Or A, Giovannoni G, Selmaj K, Tornatore C, Sweetser MT, Yang M, Sheikh SI, Dawson KT; DEFINE Study Investigators.

Source:
N Engl J Med. 2012 Sep 20;367(12):1098-107.

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