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    Home > Medical News > Medical Research Articles > FDA accepts new drug application for Sumitomo Pharmaceuticals dasotraline to treat BED

    FDA accepts new drug application for Sumitomo Pharmaceuticals dasotraline to treat BED

    • Last Update: 2020-06-08
    • Source: Internet
    • Author: User
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    recently, SumitomoPharmaceutical(http://u.Ssub-
    company(http://Sunovion Pharma announced that the U.SFood andMedicines(http://Administration (
    FDA(http://) has accepted the treatment of dasotra (dassoquer) for the treatment of moderate to severe eating disorder (BED)new drug(http://   About dasotraline
    dasotraline is a new type of dual-effect dopamine and norepinephrine reuptake inhibitor (DNRI) that inhibits pre-synaptic retake of dopamine and norepinephrine in the central nervous system (CNS) and does not stimulate the release of dopamine and norepinephrine neurons   Dasotraline is developing treatments for adults with moderate to severe BED   The pharmacokinetic characteristics of dasotraline are the ability to extend half-life and support its potential for continuous control of moderate to severe BED symptoms   Sunovion is also evaluating the drug for use in other potential indications, including attention deficit hyperactivity disorder (ADHD)   Dasotraline is a daily drug that has been shown to treat moderate to severe BED in two 12-week randomized, placebo-controlled, critical Phase III studies (SEP360-221, SEP360-321)   In clinical studies, including long-term safety studies sEP360-322, which included the evaluation of severe BED in treatment, dasotraline was found to have good tolerance
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