UK’s MHRA accepts Shire’s Elvanse filing for ADHD in adults
Ireland-headquartered drugmaker Shire (LSE: SHP) has had an application for its once-daily attention deficit/hyperactivity disorder (ADHD) drug Elvanse (lisdexamfetamine dimesylate) accepted for an adult indication.
The application was accepted by the UK’s Medicines Healthcare products Regulatory Agency (MHRA) which has agreed to act as the Reference Member State for this Decentralized Procedure, which will include the UK, Denmark and Sweden.
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