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"The grades of this revise give our conclusion that XP13512 have eventual in plonk of an potent and resourcefully tolerate conduct all for gap RLS. Our early placebo-controlled Phase 3 efficacy tribulation of XP13512, beside results announced enclosed via April 2007, demonstrated statistically principal benefits of XP13512 in treat RLS symptom completed 12 weeks. We be incited by the results of this unknown placebo-controlled Phase 3 clinical trial, which demonstrated that XP13512 be effective and across the world well-tolerated when administered to primary RLS patients for nine months," said Ronald W. Barrett, Ph.D., chief executive officer of XenoPort.
The Research Institute of the MUHC is buttress in segment by the Fonds de la recherche en santé du Québec.