Lynavoy Approved by the FDA for Cholestatic Pruritus in Patients With Primary Biliary Cholangitis
March 20, 2026
March 20, 2026
LONDON, England, March 20 -- GSK (formerly GlaxoSmithKline), a biopharmaceutical company, issued the following news release on March 19, 2026:
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Lynavoy (linerixibat) approved by the US FDA for cholestatic pruritus in patients with primary biliary cholangitis (PBC)
* Lynavoy, an ileal bile acid transporter (IBAT) inhibitor, is the first medicine approved in the US for the treatment of cholestatic pruritus in patients with PBC
* Up to 89% of . . .
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Lynavoy (linerixibat) approved by the US FDA for cholestatic pruritus in patients with primary biliary cholangitis (PBC)
* Lynavoy, an ileal bile acid transporter (IBAT) inhibitor, is the first medicine approved in the US for the treatment of cholestatic pruritus in patients with PBC
* Up to 89% of . . .
