FDA green light for Vykat XR to treat hyperphagia in PWS
The US Food and Drug Administration (FDA) has approved Soleno Therapeutics’ (Nasdaq: SLNO) Vykat (diazoxide choline) extended-release tablets, previously referred to as DCCR, for the treatment of hyperphagia in adults and children four years of age and older with Prader-Willi syndrome (PWS).
The news sent Solena’s shares rocketing more than 31% to $64.31 in after-hours trading on Wednesday.
Soleno expects Vykat XR to be available in the USA beginning in April 2025. The company also said that it has launched Soleno One, a comprehensive patient support program.
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