Nytt grönt ljus för Tremfya – ska ersätta storsäljaren Stelara

Johnson & Johnsons Tremfya får ytterligare ett FDA-godkännande. Därmed fortsätter läkemedelsjätten förverkliga sin plan om att ersätta den tidigare storsäljaren Stelara.

By Ella Käck

March 21, 2025 10:39 AM

Amerikanska läkemedelsmyndigheten FDA godkänner Tremfya (guselkumab) som läkemedel för vuxna med måttligt till svårt aktiv Crohns sjukdom. Det meddelar Johnson & Johnson (J&J) i ett pressmeddelande.

Det markerar samtidigt Tremfyas fjärde FDA-godkännande sedan läkemedlet fick ett initialt godkännande för att behandla plackpsoriasis 2017. Så sent som i september godkändes läkemedlet även för måttlig till svår ulcerös kolit.

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Nytt grönt ljus för Tremfya – ska ersätta storsäljaren Stelara

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