Previously Unexplored Population with Multiple Sclerosis Benefits from DMF
SEPTEMBER 15, 2016
At last year’s conference, which took place in Barcelona, Spain, researchers reported positive results in the DEFINE and CONFIRM phase 3 trials for Caucasian patients. The aim of the new phase 3 study was to identify the efficacy and safety outcomes for patients with relapsing MS from Asia-Pacific countries.
Over 24 weeks, the collaborative team from Japan and the United States monitored the use of DMF in 225 patients. A total of 114 patients were from Japan and the others came from South Korea, Taiwan, the Czech Republic, and Poland. The cohort was split in half to receive either DMF 240 mg or placebo twice per day.
Based on the 213 patients who completed the study, the average number of new Gd+ lesions were reduced by 84% from Weeks 12 to 24 with DMF, compared with placebo. In addition, the average number of new Gd+ lesions were reduced by 75% from Baseline to Week 24, and the average number of new or newly enlarging T2-hypointense lesions reduced by 63% at Week 24.
Adverse events were more common in those taking DMF than placebo, and common effects were gastrointestinal tolerability events (33% vs. 16%) and flushing and related symptoms (30% vs. 9%), respectively. Infection occurred in 41% on DMF and 42% on placebo.
From Baseline to Week 24, the average absolute lymphocyte counts decreased by about 16% in those treated with DMF. This kept them within normal limits at all points in the study.
“These results indicate that the beneficial effects of DMF demonstrated in Caucasian patients extend to Asian (including Japanese) MS patients,” the researchers concluded. Both efficacy and safety were confirmed in the Asia-Pacific population. The team is continuing to investigate open-label safety.
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