Long-term Extension Study of Zanubrutinib (BGB-3111) Regimens in Participants With B-cell Malignancies

Overview

The purpose of this study is to evaluate the long-term safety of zanubrutinib regimens in participants with B-cell malignancies who participated in a BeiGene parent study for zanubrutinib.

Eligibility

1. Currently participating or participated recently in a BeiGene parent study
2. Intent to continue or start zanubrutinib treatment after any of the following:
   1. At time of final analysis or study closure of the eligible BeiGene parent study
   2. At time of progressive disease (PD); and investigator, patient and medical monitor agree it is in the patient's best interest
   3. At an alternative timepoint for an alternative reason
   4. Patient who is currently on zanubrutinib treatment:

             Does not meet any protocol-specified criteria for zanubrutinib hold or permanent
             discontinuation, and, in the opinion of the investigator, will continue to benefit
             from zanubrutinib treatment
          4. Zanubrutinib-naive patient:
             Must meet the following criteria ≤ 15 days before first dose of study drug:
               1. Platelets ≥ 50,000/mm3
               2. Absolute neutrophil count ≥ 750/mm3
               3. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 x upper
                  limit of normal
               4. Serum total bilirubin ≤ 3 x upper limit of normal (not required for Gilbert
                  Syndrome)
               5. QT interval corrected for heart rate using Fridericia's formula (QTcF) ≤ 480 msec
               6. No known New York Heart Association (NYHA) Class III or IV congestive heart
                  failure
               7. Creatinine clearance ≥ 30 mL/min
          5. Female participants of childbearing potential and nonsterile males must be willing to
             use a highly effective method of birth control.
        Key Exclusion Criteria:
          1. Permanently discontinued from zanubrutinib treatment in the BeiGene parent study due
             to unacceptable toxicity, non-compliance with study procedures, or withdrawal of
             consent
          2. Uncontrolled active systemic infection or recent infection requiring parenteral
             anti-microbial therapy
          3. Life-threatening illness, medical condition or organ system dysfunction which, in the
             investigator's opinion, could compromise the participant's safety, interfere with the
             absorption or metabolism of zanubrutinib, or put the study outcomes at undue risk
          4. Concomitant chemotherapy, targeted therapy, radiation therapy, antibody-based
             therapies, or any prohibited concomitant therapy outlined in the protocol
          5. Pregnant or lactating woman
          6. Inability to comply with study procedures
          7. Concurrent participation in another therapeutic clinical study
          8. History of progressive disease (PD) while receiving a BTK inhibitor (excluding
             zanubrutinib)
        NOTE: Other protocol defined Inclusion/Exclusion criteria may apply