Ofatumumab/Methylprednisolone and Ofatumumab/Lenalidomide for Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL)

This is a phase II, single institution, and non-randomized study of patients with relapsed or
refractory CLL/SLL, utilizing a two-stage trial design. The primary endpoint for this trial
is the combined complete and partial response rate at 3 months (after the end of cycle 3) to
the protocol therapy. Investigators anticipate this trial will have a complete response and
partial response (CR+PR) rate of at least 55%.

A two-stage design is employed for this trial. The null/unacceptable CR+PR response rate is
≤35% while the anticipated true response rate to the protocol treatment is at least 55% for
each disease cohort. At the first stage, 25 patients will be accrued to the trial. If 9 or
fewer of these patients respond, then the trial will be terminated early and the response
rate to the protocol treatment will be deemed unacceptable (≤35%). Otherwise, if more than 9
patients respond during the first stage, an additional 31 patients will be enrolled to this
trial during stage 2 for a total of 56 patients. If 25 or fewer of these 56 patients respond
to the protocol treatment at the end of stage 2, no further investigation of the protocol
treatment is considered warranted. On the other hand, if more than 25 patients out of the 56
enrolled patients respond, the protocol treatment will be considered promising. If the true
response rate is ≤35%, the probability of ending the trial at stage 1 is 0.63. If, however,
the true response rate is at least 55%, then the probability of ending the trial at stage 1
is only 0.04. This two-stage design has an overall alpha level of 0.047 and a power of 0.90.

For the purpose of interim analysis at the end of stage 1, the objective response will be
measured by the end of 3 months (or end of cycle 3) from the start of the protocol treatment
prior to the initiation of the combination of ofatumumab with lenalidomide. The accrual will
not be suspended while waiting for the results of the interim analysis unless the observed
objective response rate among those patients whose objective response data are available is
below 30%.

Inclusion Criteria:

- Understand and voluntarily sign an informed consent form

- Able to adhere to the study visit schedule and other protocol requirements

- Patients must have histologically or cytologically confirmed CD5+/CD20+ B-Cell chronic
lymphocytic leukemia or small lymphocytic lymphoma. The diagnosis of CLL is based upon
the National Comprehensive Cancer Network (NCCN) guidelines. Any outside pathology
slides used as inclusion criteria for the patient will be reviewed at this institution
to confirm the diagnosis. The patient must meet all of the following CLL criteria to
participate in this study: absolute lymphocyte count > 5000/μL; CD20+ and CD5+; Bone
marrow (BM) lymphocytes ≥ 30%; Or previous confirmed diagnosis of CLL/SLL with less
than 5000/μl or less than 30% lymphocytes in BM.

- Patients are eligible if they have relapsed or refractory CLL/SLL.

- All previous cancer therapy, including radiation, hormonal therapy and surgery, must
have been discontinued at least 4 weeks prior to treatment in this study.

- Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2 at study entry

- Laboratory test results within these ranges: Absolute neutrophil count ≥ 1000/mm³,
Platelet count ≥50,000 /mm³, Renal function assessed by calculated creatinine
clearance ≥ 30ml/min by Cockcroft-Gault formula, Total bilirubin ≤ 1.5 x upper limit
of normal (ULN), aspartic transaminase (AST/SGOT) and alanine transaminase (ALT/SGPT)
≤ 2.5 x ULN, Alkaline phosphatase <2.5 x ULN

- Disease free of prior malignancies for ≥ 5 years with exception of currently treated
basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix
or breast

- All study participants must be registered into the mandatory RevAssist® program, and
be willing and able to comply with the requirements of RevAssist®.

- Females of childbearing potential (FCBP)† must have a negative serum or urine
pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days and again
within 24 hours prior to prescribing lenalidomide for Cycle 1 (prescriptions must be
filled within 7 days) and must either commit to continued abstinence from heterosexual
intercourse or begin TWO acceptable methods of birth control, one highly effective
method and one additional effective method AT THE SAME TIME, at least 28 days before
she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men
must agree to use a latex condom during sexual contact with a FCBP even if they have
had a successful vasectomy.

- Able to take aspirin (81 or 325 mg) daily as prophylactic anticoagulation (patients
intolerant to acetylsalicylic acid (ASA) may use warfarin or low molecular weight
heparin)

Exclusion Criteria:

- Any serious medical condition, laboratory abnormality, or psychiatric illness that
would prevent the patient from signing the informed consent form

- Pregnant or breast feeding females. (Lactating females must agree not to breast feed
while taking lenalidomide)

- Any condition, including the presence of laboratory abnormalities, which places the
patient at unacceptable risk if he/she were to participate in the study or confounds
the ability to interpret data from the study

- Evidence of laboratory Tumor Lysis Syndrome (TLS) by Cairo-Bishop Definition. Patients
may be enrolled upon correction of electrolyte abnormalities.

- Use of any other experimental drug or therapy within 28 days of baseline

- Known hypersensitivity to thalidomide

- The development of erythema nodosum if characterized by a desquamating rash while
taking thalidomide or similar drugs

- Any prior use of lenalidomide

- Concurrent use of other anti-cancer agents or treatments

- Known seropositive for or active viral infection with human immunodeficiency virus
(HIV)

- Positive serology for hepatitis B (HB) defined as a positive test for HBsAg. In
addition, if negative for HBsAg but HBcAb positive and HBsAb negative, a HB DNA test
will be performed and if positive the patient will be excluded. Note: If HBcAb
positive and HBsAb positive, which is indicative of a past infection, the patient can
be included. Patients who are seropositive because of hepatitis B virus vaccine are
eligible.

- Positive serology for hepatitis C (HC) defined as a positive test for hepatitis C
antibodies (HCAb), in which case reflexively perform a HC recombinant immunoblot assay
(RIBA) on the same sample to confirm the result

- Patients who have current active hepatic or biliary disease (with exception of
patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable
chronic liver disease per investigator assessment) are ineligible.

- Chronic or current infectious disease requiring systemic antibiotics, antifungal, or
antiviral treatment such as, but not limited to, chronic renal infection, chronic
chest infection with bronchiectasis, tuberculosis and active Hepatitis C

- History of significant cerebrovascular disease in the past 6 months or ongoing event
with active symptoms or sequelae

- Clinically significant cardiac disease including unstable angina, acute myocardial
infarction within 6 months prior to randomization, congestive heart failure [New York
Heart Association (NYHA) III-IV], and arrhythmia unless controlled by therapy, with
the exception of extra systoles or minor conduction abnormalities

- Significant concurrent, uncontrolled medical condition including, but not limited to,
renal, hepatic, gastrointestinal, endocrine, pulmonary, neurological, cerebral or
psychiatric disease which in the opinion of the investigator may represent a risk for
the patient