AbbVie submits for FDA approval of Venclexta and Acalabrutinib combination for untreated CLL patients
Drug Approval

AbbVie submits for FDA approval of Venclexta and Acalabrutinib combination for untreated CLL patients

The submission is supported by positive results from the Phase 3 AMPLIFY trial

  • By IPP Bureau | August 06, 2025

AbbVie has submitted a supplemental New Drug Application (sNDA) to the USFDA for a fixed-duration, all-oral combination of Venclexta  (venetoclax) and acalabrutinib for previously untreated chronic lymphocytic leukemia (CLL) patients.

The submission is supported by positive results from the Phase 3 AMPLIFY trial, where the combination significantly improved progression-free survival compared to standard chemoimmunotherapy.2

"This submission could mark a shift in frontline CLL treatment, offering patients a time-limited oral option," said Svetlana Kobina, vice president, global medical affairs, oncology, AbbVie.

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