Boehringer Ingelheim’s SPEVIGO® Receives Breakthrough Therapy Designation (BTD) from the United States Food and Drug Administration (FDA)

Boehringer Ingelheim announced that the United States Food and Drug Administration (FDA) granted Break Through Therapy Designation (BTD) to spesolimab (marketed as SPEVIGO®), an investigational treatment aimed at preventing flares in teenagers and adults suffering from generalized pustular psoriasis (GPP). Spesolimab has been granted approval by regulatory agencies for the treatment of GPP flares in nearly 40 countries.

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Boehringer Ingelheim’s SPEVIGO® Receives Breakthrough Therapy Designation (BTD) from the United States Food and Drug Administration (FDA)

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Boehringer Ingelheim’s SPEVIGO® Receives Breakthrough Therapy Designation (BTD) from the United States Food and Drug Administration (FDA)

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Shining a Spotlight on our 2022 Fellows: Get to Know the Future Leaders in Psoriasis – Mona El-Kalioby, MBBCh, MSc, MD

Psoriasis and the Pandemic: Lessons Learned from PsoProtect

Boehringer Ingelheim’s SPEVIGO® Receives Breakthrough Therapy Designation (BTD) from the United States Food and Drug Administration (FDA)

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