May 2026 AbbVie and Roche/Genentech received European Commission authorization for an expanded VENCLYXTO® (venetoclax) label, including additional combination regimens with acalabrutinib (with or without obinutuzumab) and ibrutinib for previously untreated chronic lymphocytic leukemia (CLL). The approval expands the use of venetoclax-based fixed-duration treatment approaches across European markets.
February 2026 AbbVie and Genentech (Roche Group) received U.S. FDA approval for VENCLEXTA® (venetoclax) in combination with acalabrutinib for previously untreated patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). The approval was supported by Phase III clinical data and strengthens venetoclax's position in frontline hematology treatment.