Neurocrine Biosciences Announces Publication in Orphanet Journal of Rare Diseases Advancing Understanding of Hyperphagia in Prader-Willi Syndrome
Neurocrine announced publication of expert perspectives on hyperphagia in Prader-Willi syndrome in Orphanet Journal of Rare Diseases. The manuscript frames hyperphagia as a multidimensional neurobiological condition and concludes VYKAT XR, the first FDA-approved treatment for hyperphagia in PWS, is a significant advancement best used within integrated, multidisciplinary care.
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