A Phase 1b, Multi-center, Open Label, Study to Determine the Safety and Activity of CC-292 in Combination With Rituximab in Subjects With Relapsed or Refractory Chronic Lymphocytic Leukemia / Small Lymphocytic Lymphoma.
1. Male and female subjects 18 years of age and older at the time of signing the
informed consent document.
2. Understand and voluntarily sign an informed consent document (ICD) prior to any study
related assessments/procedures being conducted.
3. Able to adhere to the study visit schedule and other protocol requirements.
4. Body weight ≥ 50 kg.
5. Must have a documented diagnosis of Chronic Lymphocytic Leukemia/Small Lymphocytic
Lymphoma (CLL/SLL) (International Workshop) guidelines for the diagnosis and
treatment of CLL (Appendix A), or lymphoma guidelines (Appendix B) for diagnosis and
treatment of SLL by investigator assessment.
6. Have failed ≥ 1 previous treatments for CLL/SLL, and have relapsed or refractory
disease following last prior treatment.
1. Refractory is defined as CLL/SLL that does not achieve at least a partial
response (PR) to therapy or that progresses within 6 months of treatment.
Relapsed CLL/SLL refers to disease that progresses after ≥ 6 months in subjects
who had achieved a PR or complete response (CR) to therapy.
2. Subjects must have failed, refused, be ineligible, or not otherwise appropriate,
per the investigator's judgment, for autologous stem cell transplant (SCT)
unless enrollment in this study is anticipated to debulk lesions in preparation
7. Eastern Cooperative Oncology Group performance status (ECOG PS) of ≤ 2
8. Life expectancy of at least 3 months form the time of signing the ICD.
9. Females of childbearing potential (FCBP)must have a negative medically supervised
pregnancy test prior to starting of study therapy.
10. Male subjects must:
1. Agree to use a condom during sexual contact with a FCBP, even if they have had a
vasectomy, throughout study drug treatment, during any dose interruption and for
28 days after end of study therapy.
2. Agree to not donate semen during study drug treatment and for 28 days after end
of study drug treatment.
11. Ability to swallow oral capsules without difficulty.
12. Have an echocardiogram or multigated acquisition scan of the heart demonstrating left
ventricular ejection fraction (LVEF) ≥ 50% or the institution's lower limit of
13. Have recovered from adverse, toxic effects of prior therapies to Grade ≤ 1 National
Cancer Institute Common Terminology Criteria for Adverse Events (NCI/CTCAE) version
4.03 except for alopecia and peripheral neuropathy. This requirement will be
subordinate to specific clinical and laboratory criteria that are otherwise
specifically addressed in these inclusion/exclusion criteria.
1. Any significant medical condition, laboratory abnormality, or psychiatric illness
that would prevent the subject from participating in the study.
2. Any condition including the presence of laboratory abnormalities, which places the
subject at unacceptable risk if he/she were to participate in the study.
3. Any condition that confounds the ability to interpret data from the study.
4. Autologous stem cell transplant within 3 months of screening date.
5. Uncontrolled intercurrent illness including, but not limited to:
1. Ongoing or active infection requiring parenteral antibiotics.
2. Uncontrolled diabetes mellitus as defined by the investigator.
3. Chronic symptomatic congestive heart failure (Class III or IV of the New York
Heart. Association Classification for Heart Disease; AppendixG).
4. Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within
6 months of signing the ICD.
5. Clinically significant cardiac arrhythmia that is symptomatic or requires
treatment, or asymptomatic sustained ventricular tachycardia. Subjects with
controlled atrial fibrillation that is asymptomatic are eligible.
6. Pregnant or lactating females.
7. Prior history of malignancies, unless the subject has been free of the disease for ≥
3 years of signing the informed consent. Exceptions to the ≥ 3 year time limit
include history of the following:
1. Basal cell carcinoma of the skin.
2. Squamous cell carcinoma of the skin.
3. Carcinoma in situ of the cervix.
4. Carcinoma in situ of the breast.
5. Carcinoma in situ of the bladder.
6. Incidental histologic finding of prostate cancer (TNM stage of T1a or T1b). (The
TNM staging system is based on the extent of the tumor (T), whether cancer cells
have spread to nearby (regional) lymph nodes (N), and whether distant (to other
parts of the body) metastasis (M) has occurred).
8. Known seropositivity for or history of active viral infection with Human
Immunodeficiency Virus (HIV).
9. Seropositive for or active viral infection with Hepatitis B virus (HBV):
1. HBV surface antigen positive.
2. HBV surface antigen negative, HBV surface antibody positive and/or HBV core
antibody positive and detectable viral deoxyribonucleic acid (DNA).
Note: Subjects who are HBV surface antigen negative and viral DNA negative are
3. Subjects who had HBV but have received an antiviral treatment and show no
detectable viral DNA within 6 months of signing the ICD are eligible.
4. Subjects who exhibit the classical vaccination profile of HBV surface antibody
positive, HBV core antibody negative, and HBV surface antigen negative are
10. Known seropositivity for or active viral infection with Hepatitis C virus (HCV).
11. Subjects who are at a high risk for a thromboembolic event and are not willing to
take venous thromboembolic event (VTE) prophylaxis.
12. Any of the following laboratory abnormalities:
1. Absolute neutrophil count (ANC) ≤ 1,000 cells/mm3 (1.0 x 109/L) unless secondary
to bone marrow involvement by lymphoma as demonstrated by recent bone marrow
aspiration and bone marrow biopsy.
2. Platelet count ≤ 50,000/mm3 (50 x 109/L) unless secondary to bone marrow
involvement by lymphoma as demonstrated by recent bone marrow aspiration and
bone marrow biopsy. Note that growth factors or transfusions should not be
administered during screening for the sole purpose of helping a subject exceed
these exclusionary laboratory values.
3. Serum Aspartate Transaminase/Serum Glutamic Oxaloacetic Transaminase (AST/SGOT)
or Alanine Transaminase/Serum Glutamic Pyruvate Transaminase (ALT/SGPT) > 3.0 x
Upper Limit of Normal (ULN) or > 5.0 x ULN in cases of documented liver
involvement by lymphoma.
4. Serum bilirubin > 1.5 x ULN or > 3.0 x ULN in cases of Gilbert's Syndrome and
documented liver involvement by lymphoma.
5. Calculated creatinine clearance using the Cockcroft-Gault formula (Cockcroft,
- For subjects enrolling in Part 1 creatinine clearance value must be < 30
- For subjects enrolling in Part 2 creatinine clearance value must be < 60
6. Corrected QT interval (QTc) prolongation (defined as a QTc > 450 msec for males
and > 470 msec for females [Fridericia's correction] echocardiograms (ECGs) or
other clinically significant ECG abnormalities as assessed by the investigator.
An average of 3 QTc intervals may be obtained if necessary.
7. Evidence of Tumor Lysis Syndrome (TLS) per the Cairo-Bishop definition of
laboratory TLS ([Appendix F] subjects may be enrolled upon correction of
13. Prior exposure to Bruton Tyrosine Kinase inhibitors.
14. Chemotherapy, radiotherapy, investigational anti cancer therapy or major surgery
within 28 days of Day 1 dosing.
15. Use of systemic corticosteroids in doses greater than prednisone equivalent 20 mg/day
within 3 weeks prior to the first dose of study drug treatment.
16. Concomitant use of medicines known to cause QT prolongation or torsades de pointes
17. Chronic use of H2 antagonists or proton pump inhibitors or their use within 7 days of
first dose of study drug treatment. Subjects with chronic gastroesophageal reflux
disease, dyspepsia, and peptic ulcer disease, should be carefully evaluated for their
suitability for this treatment prior to enrollment in this study.
18. Gastrointestinal abnormalities including the ability to take oral medication, require
intravenous (IV) alimentation, or prior surgical procedures affecting absorption.
19. History of hypersensitivity reaction to Rituximab.
20. Any vaccinations incorporating the use of a live vaccine within 3 weeks from first