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    Home > Medical News > Latest Medical News > UCB Fintepla Receives FDA Approval for Expanded Indications

    UCB Fintepla Receives FDA Approval for Expanded Indications

    • Last Update: 2022-05-26
    • Source: Internet
    • Author: User
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    On March 28, 2022, UCB (UCB) announced that the U.


    LGS is a severe childhood-onset developmental and epileptic encephalopathy (DEE) characterized by a high incidence of drug-refractory seizures and severe impairment of neurodevelopmental, cognitive, and motor function


    Fintepla is a low-dose fenfluramine in liquid form


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    The Phase 3 clinical trial enrolled 263 LGS patients (age range: 2-35 years)


    References:

    [1] US FDA Approves FINTEPLA® ▼(fenfluramine) Oral Solution for Treatment of Seizures Associated with Lennox-Gastaut Syndrome (LGS).


    Note: The original text has been deleted

    Original title: Express | Approved again in the field of epilepsy, the prospect of fenfluramine "old drug new" can be expected

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