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FDA Approves VYVANSE(TM) (lisdexamfetamine Dimesylate), The First And Only Once-Daily Prodrug Stimulant To Treat ADHD In Adults

BASINGSTOKE, England and PHILADELPHIA, April 23 /PRNewswire/ -- - Within the First Eight Months Since its Introduction in the United States, VYVANSE has Achieved Over One Million Prescriptions - In a Clinical Study With Adults, VYVANSE was Shown to Significantly Improve the Symptoms of ADHD (Inattention, Hyperactivity and Impulsivity)(1)
United States Johns Hopkins University Lisdexamfetamine Dimesylate Matthew Emmens Davidw Goodman Shire Plc

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Stoke Therapeutics Presents New In-Vivo Data That Demonstrated Dose-Related Target Engagement and OP

โ€“ Data presented at the Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting support the Companyโ€™s work to advance STK-002 as the first potential disease modifying treatment for Autosomal Dominant Optic Atrophy (ADOA) โ€“โ€“ ADOA is the most common inherited optic nerve disorder โ€“BEDFORD, Mass.--(B...
United Kingdom United States Edwardm Kaye Eric Rojas Karen Anderson Augmentation Of Nuclear Gene Output

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