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About
This is a multicentric international phase III, double blind randomized study assessing efficacy and safety in parallel group of BF2.649 (pitolisant) compared to placebo in add-on to sodium oxybate of narcoleptic patients with residual Excessive Daytime Sleepiness (EDS) during 8 weeks
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Interventional model
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51 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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