Inclusion Criteria:

          -  Diagnosis of CLL or small lymphocytic lymphoma (SLL) meeting International Workshop on
             Chronic Lymphocytic Leukemia (IWCLL) 2008 criteria AND biopsy proven transformation to
             diffuse large B cell lymphoma (DLBCL), clinically consistent with Richter?s syndrome
             (RS) OR histologically diagnosed relapsed or refractory DLBCL including transformed
             follicular lymphoma (tFL) ineligible for or refractory to platinum containing salvage
             therapy for the dose escalation portion of the study. For the dose expansion phase
             only patients with CLL with transformation to DLBCL or tFL will be eligible

          -  Eastern Cooperative Oncology Group (ECOG) performance status 0-2

          -  Absolute neutrophil count (ANC) >= 500/uL

          -  Platelet count >= 30,000/uL (unless due to bone marrow involvement)

          -  Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 2.5 ULN

          -  Total bilirubin =< 1.5 ULN (unless due to liver involvement, hemolysis, or Gilbert?s
             disease)

          -  Creatinine clearance >= 40 mL/min (Cockcroft-Gault estimated)

          -  Women of childbearing potential and men who are sexually active must be practicing a
             highly effective method of birth control during and after the study consistent with
             local regulations regarding the use of birth control methods for subjects
             participating in clinical trials. Men must agree to not donate sperm during and after
             the study. For females, these restrictions apply for 1 month after the last dose of
             study drug. For males, these restrictions apply for 3 months after the last dose of
             study drug

          -  Women of childbearing potential must have a negative serum (beta-human chorionic
             gonadotropin [beta-hCG]) or urine pregnancy test at screening. Women who are pregnant
             or breastfeeding are ineligible for this study

          -  Patients must sign an informed consent document indicating that they understand the
             purpose of and procedures required for the study, including biomarkers, and are
             willing to participate in the study

        Exclusion Criteria:

          -  Documented infection with human immunodeficiency virus (HIV) or chronic, active
             hepatitis B or C infection

          -  Any chemotherapy or monoclonal antibodies within 14 days or kinase inhibitors (except
             BTKi) within 5 half-lives before cycle 1, day 1 (C1D1). BTK inhibitors may be
             continued until 2 days prior to C1D1. Steroids are allowed for palliation of symptoms
             due to lymphoma

          -  Toxicity from previous therapy which has not resolved to grade 1 (or patient?s
             previous baseline)

          -  Other active malignancies except those treated with curative intent with no active
             disease at the time of study entry or those felt to be at low risk of progression or
             recurrence over the next 2 years (such as low risk prostate cancer on active
             surveillance)

          -  New York Heart Association (NYHA) class III/IV heart disease or other significant
             medical condition or organ system dysfunction which could compromise the subject?s
             safety or put the study outcomes at undue risk

          -  Uncontrolled systemic infection

          -  Unable to swallow capsules or significant malabsorption syndrome, symptomatic
             inflammatory bowel disease or ulcerative colitis, or partial or complete bowel
             obstruction at the time of screening

          -  Patients who are pregnant or breastfeeding

          -  Patients with known central nervous system (CNS) involvement by CLL or lymphoma

          -  Patients who have underwent autologous or allogeneic stem cell transplant =< 4 weeks
             prior to C1D1 or have active graft-versus-host disease are excluded