Front-line VenObi Combination Followed by Ven or VenZan Combination in Patients With Residual Disease: a MRD Tailored Treatment for Young Patients With High-risk CLL

Exclusion Criteria

• •1. Any significant concurrent, uncontrolled medical condition or organ system dysfunction and laboratory abnormality or psychiatric disease, which, in the investigator's opinion, could compromise the subject's safety or put the study outcomes at undue risk or prevent the subject from signing the informed consent form.
• •2. Known active histological transformation from CLL to an aggressive lymphoma (i.e., Richter's transformation or pro-lymphocytic leukemia);
• •3. known central nervous system involvement.
• •4. Active malignancy or systemic therapy for another malignancy within 3 years
• •Except:
• •Malignancies surgically treated with curative intent and with no known active disease present for ≥ 3 years before randomization
• •Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease
• •Adequately treated cervical carcinoma in situ without evidence of disease
• •Surgically/adequately treated low grade, early stage localized prostate cancer without evidence of disease
• •5\. Co-morbidities:
• •Uncontrolled autoimmune hemolytic anemia or thrombocytopenia
• •Any uncontrolled illness that in the opinion of the investigator would preclude administration of study therapy
• •History of stroke or intracranial hemorrhage within 180 days before first dose of study drug.
• •History of severe bleeding disorder or history of spontaneous bleeding requiring blood transfusion or other medical intervention due to thrombocytopenia or inherited or acquired bleeding disorders due to deficiency or functional abnormality of any coagulation proteins.
• •History of significant cardiovascular disease, defined as:
• •1. Congestive heart failure greater than New York Heart Association (NYHA) class II according to the NYHA functional classification.
• •2. Unstable angina or myocardial infarction with 6 months of enrollment.
• •3. Serious cardiac arrhythmia or clinically significant ECG abnormality: corrected QT wave (QTcF) \> 480 msec based on the Fridericia's formula or other ECG abnormalities including second-degree atrioventricular block type II, third-degree atrioventricular block. Participants who have a pacemaker will be allowed on study despite ECG abnormalities or the inability to calculate the QTc.
• •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
• •History of tuberculosis within the last five years or recent exposure to tuberculosis equal to or less than 6 months.
• •History of progressive multifocal leukoencephalopathy (PML)
• •History of HIV infection or active hepatitis B (chronic or acute) or hepatitis C infection 1. 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 take appropriate anti-viral prophylaxis as indicated and undergo monthly DNA testing.
• •2\. Patients positive for hepatitis C virus (HCV) antibody are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA.
• •Inadequate renal function: CrCl \< 30 mL/min.
• •Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis.
• •History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies or known sensitivity or allergy to murine products
• •Known intolerance or hypersensitivity to any of the components of the therapeutic regimen
• •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.
• •Prior major surgical procedure within 4 weeks of study, or anticipation of need for a major surgical procedure during the course of the study
• •Known condition or other clinical situation that would affect oral absorption.
• •Psychiatric illness/social situations that would interfere with study compliance.
• •Inability to swallow a large number of tablets.
• •6\. Concomitant medications and drug interactions:
• •Patients who are on treatment with the following agents within 7 days prior to treatment:
• •Strong CYP3A inhibitors such as fluconazole, ketoconazole, and clarithromycin Strong CYP3A inducers such as rifampin, carbamazepine and strong inhibitors or inducers of CYP2C8, CYP2C9 and CYP2C19. The same applied for moderate inhibitors or inducers of CYP3A Requires warfarin, marcumar, or phenprocoumon (due to potential drug-drug interactions that may potentially increase the exposure of warfarin or phenprocoumon)
• •Prior anti-CD20 monoclonal antibody therapy for non-malignant indication
• •7\. Females who are currently pregnant or breastfeeding.
• •8\. Participation in a separate investigational therapeutic study unless authorized by the investigator.