FDA approves AbbVie Venclexta and acalabrutinib combo for previously untreated CLL patients

Reuters02-20 15:00
FDA approves AbbVie Venclexta and acalabrutinib combo for previously untreated CLL patients

AbbVie Inc. said the U.S. Food and Drug Administration approved a supplemental new drug application for the all-oral, fixed-duration combination of VENCLEXTA (venetoclax) and acalabrutinib to treat previously untreated adult patients with chronic lymphocytic leukemia. The approval was supported by data from the Phase 3 AMPLIFY trial.

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: 202602200200PR_NEWS_USPR_____CG92191) on February 20, 2026, and is solely responsible for the information contained therein.

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