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FDA approves AbbVie venclexta, acalabrutinib supplemental new drug application

AbbVie (ABBV) announced that the FDA has approved a supplemental new drug application for the combination regimen of venclexta and acalabrutinib for the treatment of previously untreated adult patients with chronic lymphocytic leukemia. The approval is supported by data from the Phase 3 AMPLIFY trial.

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