Rozšířený přístupový program pro Pirtobrutinib pro účastníky s rakovinou B-buněk

Inclusion Criteria:

• Have been diagnosed with:

  • CLL or SLL and have received treatment with the following five classes of therapy: Chemotherapy, anti-cluster of differentiation (anti-cd) 20 antibody, covalent Bruton's tyrosine kinase (BTK) inhibitor, B-cell lymphoma-2 (BCL-2) inhibitor, and phosphatidylinositol 3-kinase (PI3K) inhibitor
  • MCL that has been previously treated with a covalent BTK inhibitor
  • Richter's Transformation (RT) with previous Richter's directed-therapy
  • Waldenstrom macroglobulinemia (WM), previously treated with chemotherapy, anti-CD20 antibody and a covalent BTK inhibitor

• Are not eligible for an ongoing pirtobrutinib clinical trial

Exclusion Criteria:

• Inadequate organ function
• Significant cardiovascular disease
• History of allogenic or autologous stem cell transplant (SCT) or chimeric antigen receptor modified Tcell (CAR-T) therapy within 60 days
• Tested positive for human immunodeficiency syndrome (HIV) or known active hepatitis B or C virus or cytomegalovirus (CMV) infection
• Active, uncontrolled autoimmune cytopenia
• Clinically significant active malabsorption syndrome
• Participants requiring therapeutic anticoagulation with warfarin or another vitamin K antagonist