FDA clears AbbVie’s Decnupaz for rare blood cancer
The US Food and Drug Administration has approved US pharma AbbVie’s (NYSE: ABBV) Decnupaz (pivekimab sunirine-pvzy) for adults with blastic plasmacytoid dendritic cell neoplasm, a rare and aggressive blood cancer.
The May 27 approval followed a priority review. Decnupaz had also received breakthrough therapy and orphan drug designations, giving AbbVie a quicker regulatory path in a small disease area with limited treatment options.
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