Germanys' Merck KGaA presented results showing that its oral cancer drug Cladribine (cladribine) caused a significant reduction in the rate of clinical relapses, disability progression and brain lesions, as well as a significant increase in the proportion of patients who remained relapse-free, when used as a therapy for relapsing-remitting multiple sclerosis, at the annual meeting of the American Academy of Neurology, held in Seattle, Washington.
If launched onto the market, the drug could become the first MS medicine that does not have to be injected. Merck hopes to apply for the additional indication before the end of the year.
The results from both Cladribine treatment groups in the study demonstrated a statistically-significant reduction in the annualized rate of relapses compared to placebo. Patients treated with the low-dose regimen of the drug experienced a 58% relative reduction in annualized relapse rates with respect to placebo (0.14 versus 0.33 for the placebo group; p<0.001). Patients in the high-dose regimen group experienced a 55% relative reduction in annualized relapse rates with respect to placebo (0.15 vs 0.33; p<0.001).
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