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BioWorld - Sunday, March 22, 2026
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Home » Boehringer grabs first FDA approval in rare form of psoriasis
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Boehringer grabs first FDA approval in rare form of psoriasis

Sep. 2, 2022
By Jennifer Boggs and Richard Staines
The U.S. FDA has become the first global regulator to approve Boehringer Ingelheim GmbH’s spesolimab, the first treatment specifically approved for generalized pustular psoriasis flares in adults, a rare and potentially fatal disease. Branded as Spevigo, it works by inhibiting interleukin-36 and is delivered via intravenous injection. Ingelheim, Germany-based Boehringer Ingelheim is not giving away details about pricing but Carinne Brouillon, a member of the company’s board responsible for human pharma, said Spevigo is “priced similarly to the other biologic therapies used to treat rare dermatologic diseases.”
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