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      Regeneron's Arcalyst Receives Orphan Drug Status from FDA and European Commission

      Regeneron Pharmaceuticals' drug Arcalyst has been granted orphan drug status by both the U.S. Food and Drug Administration (FDA) and the European Commission. This designation, awarded in 2021, is intended for medications that address diseases affecting small patient populations.

      Kiniksa Pharmaceuticals licensed Arcalyst from Regeneron in 2017. The orphan drug designation highlights the importance of developing treatments for rare conditions, providing incentives for companies to invest in these specialized therapies.

      © 2026 KLEA News. All Rights Reserved. This article is provided for informational purposes only. It is not offered or intended to be used as legal, tax, investment, financial, or other advice.

      Source: KLEA News

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