Approval of Vykat XR marks the first treatment indicated for hyperphagia in patients with Prader-Willi syndrome.
PANTHERx® Rare, a leader in rare disease product patient access and support services in the United States, is pleased to ...
Soleno expects VYKAT XR to be available in the U.S. beginning in April 2025. “The approval of VYKAT XR is a significant ...
The US Food and Drug Administration (FDA) has approved Soleno Therapeutics’ Vykat XR (diazoxide choline) extended-release ...
Vykat XR is specifically indicated to address hyperphagia, or the abnormally strong sensation of hunger, which often leads to ...
Since 2000, when the FDA approved recombinant human growth hormone (rhGH) for those with the rare genetic disorder ...
Soleno Therapeutics (SLNO) “announced that the FDA has approved VYKAT XR, diazoxide choline, extended-release tablets, previously referred to ...
US FDA approves Soleno Therapeutics’ Vykat XR to treat hyperphagia in Prader-Willi syndrome: Redwood City, California Saturday, March 29, 2025, 18:00 Hrs [IST] Soleno Therapeuti ...
This outcome represents a best-case scenario for Soleno, as it aligns with expectations and provides a strong foundation for the drug’s commercial launch. VYKAT XR is set to enter the U.S ...