PureTech unit Akili gains FDA clearance of EndeavorRx for children with ADHD

16 June 2020
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London-listed biotech firm PureTech Health’s (LSE: PRTC) founded entity, Akili Interactive, has gained US Food and Drug Administration clearance for EndeavorRx (AKL-T01) as a prescription treatment for children with attention-deficit/hyperactivity disorder (ADHD).

News of the approval saw PureTech’s shares rise 10.2% to 264.50 pence by mid-afternoon today.

Delivered through a captivating video game experience, EndeavorRx is indicated to improve attention function as measured by computer-based testing in children aged eight-12 years old with primarily inattentive or combined-type ADHD, who have a demonstrated attention issue. Persistent attention issues have a significant impact on the daily lives of millions of people.

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