Background Schaaf-Yang syndrome (SYS) is caused by truncating mutations in MAGEL2, mapping to the Prader-Willi region (15q11-q13), with an ... and Hospital Sant Joan de Déu (PIC-111-19). We would like ...
The FDA has approved Vykat XR (diazoxide choline) for the treatment of hyperphagia in adults and pediatric patients 4 years ...
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News-Medical.Net on MSNUS FDA approves first treatment for hyperphagia in Prader-Willi syndromeThe United States Food and Drug Administration (US FDA) has approved VYKATâ„¢ XR, a significant milestone as the first approved treatment for hyperphagia in Prader-Willi syndrome (PWS).
Clearance of Vykat unlocks what analysts anticipate will be a lucrative market opportunity for Soleno Therapeutics.
Federal regulators are clearing a first-of-its-kind treatment for symptoms of a rare neurodevelopmental disorder that is ...
The FDA has approved the first therapy to address hyperphagia for children and adults aged 4 years and older with ...
The U.S. Food and Drug Administration on Wednesday approved Soleno Therapeutics' drug to treat a rare genetic disorder, ...
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MedPage Today on MSNFDA OKs First Drug for Hyperphagia in Prader-Willi SyndromeDiazoxide choline is the first drug indicated for hyperphagia in the rare genetic disorder. Prior to approval, people with ...
Credit: Solano Therapeutics. Vykat XR contains an extended-release formulation of diazoxide choline, the crystalline salt of diazoxide. Vykat XR is expected to be available in April 2025.
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