FDA approves AbbVie DECNUPAZ for adult BPDCN treatment

AbbVie, Inc.

AbbVie, Inc.

ABBV

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  • AbbVie won FDA clearance for DECNUPAZ (pivekimab sunirine-pvzy) to treat adult BPDCN, an ultra-rare aggressive blood cancer.
  • Approval rests on the Phase 1/2 CADENZA trial; newly diagnosed patients showed a 69.7% composite complete response rate.
  • Label includes a boxed warning for hepatotoxicity, including hepatic veno-occlusive disease.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. AbbVie Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202605271818PR_NEWS_USPR_____CG69114) on May 27, 2026, and is solely responsible for the information contained therein.

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