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