Neurocrine expands into metabolic diseases with $2.9 billion Soleno buyout

Industry:    3 days ago

Neurocrine Biosciences will acquire rare-disease drugmaker Soleno Therapeutics for $2.9 billion in cash, the companies said on Monday, marking the neuroscience-focused drugmaker’s expansion into metabolic disorders.

The deal ​gives Neurocrine access to Vykat XR, the first drug approved in the U.S. to ​treat hyperphagia associated with Prader-Willi syndrome, a rare genetic disorder.

Neurocrine currently ⁠markets two rare-disease drugs, Ingrezza and Crenessity, which brought in combined sales of $2.81 billion ​in 2025.

The acquisition adds a “third leg to the story that plays into Neurocrine’s current ​capabilities,” RBC Capital analyst Brian Abrahams said, noting its “accretion potential and competitive positioning”.

Neurocrine has offered $53 per Soleno share held, which represents a premium of about 34% to the stock’s last close.

Soleno shares surged ​nearly 33% in early trading.

Vykat XR is “a potential blockbuster in the making,” Neurocrine CEO ​Kyle Gano said on a call with analysts, though he added the company currently has no ‌plans ⁠to launch the drug in Europe as it focuses on the U.S. market.

Cantor analyst Josh Schimmer expects Vykat XR to surpass $1 billion in annual sales in 2029.

The treatment generated about $190 million in sales in 2025, within roughly nine months after receiving approval in March.

The ​deal, which is expected ​to close in ⁠the next 90 days, will be funded with cash on hand, Neurocrine said, adding that it plans to take a modest ​amount of prepayable debt.

Hyperphagia, or feelings of intense and persistent hunger, ​is the ⁠hallmark symptom of Prader-Willi syndrome, which could lead to severe obesity as well as physical, mental and behavioral problems.

CEO Gano said the company was not necessarily aiming for weight ⁠loss with ​Vykat XR, but noted that starting patients at ​a younger age and lower BMI could help maintain weight over time, something it would consider going forward.

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