A Study of Venetoclax and Rituximab/Hyaluronidase Human in Relapsed/Refractory CLL

The study has one arm and all the patients will receive venetoclax and rituximab.

Inclusion Criteria:

- Signed Informed Consent Form

- Ability and willingness to comply with the requirements of the study protocol

- Patient must have diagnosis of CLL that meets published 2008 IWCLL NCI-WG criteria.

- Patient must have relapsed/refractory disease with an indication for treatment.

- Patient must have an Eastern Cooperative Oncology Group (ECOG) performance score of ≤
2

- Adequate hematologic function (unless caused by underlying disease, as established by
extensive bone marrow involvement or as a result of hypersplenism secondary to the
involvement of the spleen by lymphoma per the investigator) defined as follows:

- Hemoglobin (> / =) 9 g/dL

- Absolute neutrophil count (> / =) 1.0 x 109/L

- Platelet count (> / =)75 x 109/L

- Adequate renal function, as indicated by:

- Calculated creatinine clearance ≥ 30 mL/min using 24-hour Creatinine Clearance or
modified Cockcroft-Gault equation (eCCR; with the use of ideal body mass [IBM]
instead of mass)

- Adequate liver function, as indicated by:

- AST or ALT (< / =) 2.5 x ULN

- Total bilirubin < 1.5 x ULN (or (< / =) 3 x ULN for patients with documented
Gilbert syndrome)

- Female patients who are not of child-bearing potential and female patients of
child-bearing potential who have a negative serum pregnancy test within 3 days prior
to Cycle 1, Day 1.

- Patients with HIV infection could be included in the study, as long as their disease
is under control on anti-retroviral therapy. Precautions should be taken to modify
their HAART regimen to minimize drug interaction

- Warfarin is considered a cautionary medication. Patients on warfarin will be
encouraged to replace warfarin with other anticoagulants if possible. If it is not
possible or patient is not willing to switch, they could still be included in the
study with caution.

Exclusion Criteria:

- Known hypersensitivity to any of the study drugs

- Allogeneic stem cell transplant within the past 1 year.

- Richter's transformation confirmed by biopsy

- History of other malignancy that could affect compliance with the protocol or
interpretation of results

- Patients with a history of curatively treated basal or squamous cell carcinoma or
Stage 1 melanoma of the skin or in situ carcinoma of the cervix are eligible.

- Patients with a malignancy that has been treated with surgery alone with curative
intent will be included. Individuals in documented remission without treatment
for (> / =) 2 years prior to enrollment may be included at the discretion of the
investigator.

- Evidence of significant, uncontrolled concomitant diseases that could affect
compliance with the protocol or interpretation of results or that could increase risk
to the patient, including renal disease that would preclude chemotherapy
administration or pulmonary disease (including obstructive pulmonary disease and
history of bronchospasm)

- Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection
(excluding fungal infections of nail beds) at study enrollment, or any major episode
of infection requiring treatment with IV antibiotics or hospitalization (relating to
the completion of the course of antibiotics) within 4 weeks prior to Cycle 1, Day 1

- Received the following agents within 7 days prior to the first dose of venetoclax:

- Steroid therapy for anti-neoplastic intent

- Strong and moderate CYP3A inhibitors

- Strong and moderate CYP3A inducers

- Consumed grapefruit, grapefruit products, Seville oranges (including marmalade
containing Seville oranges), or star fruit within 3 days prior to the first dose
of venetoclax

- Clinically significant history of liver disease, including viral or other hepatitis,
current alcohol abuse, or cirrhosis

- Presence of positive test results for hepatitis B virus (HBV), hepatitis B surface
antigen (HBsAg), or hepatitis C (HCV) antibody

- Patients who are positive for HCV antibody must be negative for HCV by polymerase
chain reaction (PCR) to be eligible for study participation

- Patients with occult or prior HBV infection (defined as positive total hepatitis B
core antibody [HBcAb] and negative HBsAg) may be included if HBV DNA is undetectable.
These patients must be willing to undergo monthly DNA testing.

- Known infection with human T-cell leukemia virus 1 (HTLV-1)

- Patients with uncontrolled HIV infection

- Receipt of live-virus vaccines within 28 days prior to the initiation of study
treatment or need for live-virus vaccines at any time during study treatment

- Pregnant or lactating, or intending to become pregnant during the study Women of
childbearing potential must have a negative serum pregnancy test result within 21 days
prior to initiation of study drug.

- Recent major surgery (within 6 weeks prior to the start of Cycle 1, Day 1) other than
for diagnosis

- Malabsorption syndrome or other condition that precludes enteral route of
administration

- Known allergy to both xanthine oxidase inhibitors and rasburicase