Safety Study of CC-292 and Rituximab in Subjects With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Completed · Phase 1

Conditions studied: Leukemia Lymphocytic Chronic B-Cell

In brief

This is a dose finding study using a 3 + 3 dose escalation and expansion design to determine a Not Tolerated Dose (NTD), Optimal Biological Effect Dose (OBE) and / or Maximum Tolerated Dose (MTD). These data will be used to establish a Recommended Phase 2 Dose (RP2D) for the combination of CC-292 and Rituximab in subjects with CLL.

Key facts

Study ID: NCT01744626
Run by: Celgene Corporation
People needed: 40
Starts: 2012-12-01
Expected to finish: 2015-12-01
Last updated by the study team: 2016-04-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male and female subjects 18 years of age and older at the time of signing the informed consent document.
Understand and voluntarily sign an informed consent document (ICD) prior to any study related assessments/procedures being conducted.
Able to adhere to the study visit schedule and other protocol requirements.
Body weight ≥ 50 kg.
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.
Have failed ≥ 1 previous treatments for CLL/SLL, and have relapsed or refractory disease following last prior treatment.
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.
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 for SCT.
Eastern Cooperative Oncology Group performance status (ECOG PS) of ≤ 2
Life expectancy of at least 3 months form the time of signing the ICD.
Females of childbearing potential (FCBP)must have a negative medically supervised pregnancy test prior to starting of study therapy.
Male subjects must:
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.
Agree to not donate semen during study drug treatment and for 28 days after end of study drug treatment.
Ability to swallow oral capsules without difficulty.
Have an echocardiogram or multigated acquisition scan of the heart demonstrating left ventricular ejection fraction (LVEF) ≥ 50% or the institution's lower limit of normal.
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.

You may not qualify if…

Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study.
Any condition that confounds the ability to interpret data from the study.
Autologous stem cell transplant within 3 months of screening date.
Uncontrolled intercurrent illness including, but not limited to:
Ongoing or active infection requiring parenteral antibiotics.
Uncontrolled diabetes mellitus as defined by the investigator.
Chronic symptomatic congestive heart failure (Class III or IV of the New York Heart. Association Classification for Heart Disease; AppendixG).
Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within 6 months of signing the ICD.
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.
Pregnant or lactating females.
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:
Basal cell carcinoma of the skin.
Squamous cell carcinoma of the skin.
Carcinoma in situ of the cervix.
Carcinoma in situ of the breast.
Carcinoma in situ of the bladder.
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).
Known seropositivity for or history of active viral infection with Human Immunodeficiency Virus (HIV).
Seropositive for or active viral infection with Hepatitis B virus (HBV):
HBV surface antigen positive.
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 eligible.
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.
Subjects who exhibit the classical vaccination profile of HBV surface antibody positive, HBV core antibody negative, and HBV surface antigen negative are eligible.

Where it is running

Clearview Cancer Institute — Huntsville, Alabama, United States
Horizon Oncology Research, Inc — Lafayette, Indiana, United States
Hackensack UMC — Hackensack, New Jersey, United States
The West Clinic — Memphis, Tennessee, United States
Universitätsklinik Ulm — Ulm, Bavaria, Germany
Städt. Klinikum München-Schwabing — Bayern, Germany
Universitatsklinikum Wurzburg — Bayern, Germany
Universitätsklinik Köln — Cologne, Germany

Full record on ClinicalTrials.gov

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