Soleno said VYKAT XR was approved by the FDA in March 2025 for hyperphagia in adults and pediatric patients aged 4 years and older with Prader-Willi syndrome. The company reported net revenue of USD 190.4 million for the year ended Dec. 31, 2025, and cash of USD 506.1 million at Dec. 31, 2025. Soleno also reported positive net income of USD 20.9 million for the year ended Dec. 31, 2025. Launch metrics cited include 859 active patients and a discontinuation rate due to adverse events of about 12% as of end of day Dec. 31, 2025. Soleno said it announced a USD 100 million stock repurchase in November 2025.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Soleno Therapeutics Inc. published the original content used to generate this news brief on March 18, 2026, and is solely responsible for the information contained therein.
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