A Randomized, Multicenter, Open-Label, Non-Inferiority, Phase 3 Study of ACP-196 Versus Ibrutinib in Previously Treated Subjects with High Risk Chronic Lymphocytic Leukemia
- Conditions
- High Risk Chronic Lymphocytic LeukemiaMedDRA version: 21.0Level: LLTClassification code 10008976Term: Chronic lymphocytic leukemiaSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2014-005530-64-PL
- Lead Sponsor
- Acerta Pharma B.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 500
•Men and women = 18 years of age.
•Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
•Diagnosis of CLL that meets published diagnostic criteria (Hallek 2008):
oMonoclonal B-cells (either kappa or lambda light chain restricted) that are clonally co-expressing = 1 B-cell marker (CD19, CD20, or CD23) and CD5.
oProlymphocytes may comprise = 55% of blood lymphocytes.
oPresence of = 5 x 10^9 B lymphocytes/L (5000 µL) in the peripheral blood (at any point since diagnosis); this applies to CLL only.
•Must have = 1 of the following high-risk prognostic factors:
oPresence of 17p del by central laboratory
oPresence of 11q del by central laboratory
•Active disease meeting = 1 of the following IWCLL 2008 criteria for requiring treatment:
Evidence of progressive marrow failure as manifested by the development of, or worsening of, anemia (hemoglobin < 10 g/dL) and/or thrombocytopenia (platelets < 100,000/µL).
oMassive (ie, = 6 cm below the left costal margin), progressive, or symptomatic splenomegaly
oMassive nodes (ie, = 10 cm in the longest diameter), progressive, or symptomatic lymphadenopathy.
oProgressive lymphocytosis with an increase of > 50% over a 2-month period or a lymphocyte doubling time (LDT) of < 6 months. LDT may be obtained by linear regression extrapolation of absolute lymphocyte counts (ALC) obtained at intervals of 2 weeks over an observation period of 2 to 3 months. In subjects with initial blood lymphocyte counts of < 30 X 10^9/L (30,000/µL), LDT should not be used as a single parameter to define indication for treatment. In addition, factors contributing to lymphocytosis or lymphadenopathy other than CLL (eg, infections) should be excluded.
oAutoimmune anemia and/or thrombocytopenia that is poorly responsive to standard therapy.
oConstitutional symptoms documented in the subject’s chart with supportive objective measures, as appropriate, defined as = 1 of the following disease related symptoms or signs:
Unintentional weight loss = 10% within the previous 6 months before Screening.
Significant fatigue (ie, ECOG performance status 2 or worse; inability to work or perform usual activities).
Fevers higher than 100.5°F or 38.0°C for 2 or more weeks before Screening without evidence of infection.
Night sweats for > 1 month before Screening without evidence of infection.
•Must have received = 1 prior therapies for CLL.
•Meet the following laboratory parameters:
oAbsolute neutrophil count (ANC) = 750 cells/µL (0.75 x 10^9/L) or = 500 cells/µL (0.50 x 10^9/L) in subjects with documented bone marrow involvement and independent of growth factor support 7 days before assessment.
oPlatelet count = 30,000 cells/µL (30 x 10^9/L) without transfusion support 7 days before assessment. Subjects with transfusion-dependent thrombocytopenia are excluded.
oSerum aspartate transaminase (AST/SGOT) and alanine transaminase (ALT/SGPT) = 3.0 x upper limit of normal (ULN).
oTotal bilirubin = 1.5 x ULN.
oEstimated creatinine clearance (ie, estimated glomerular filtration rate [eGFR] using Cockcroft-Gault) = 30 mL/min.
•Able to receive all outpatient treatment, all laboratory monitoring, and all radiologic evaluations at the institution that administers study drug for the entire study.
•Women who are sexually active and can bear children must agree to use highly effective
forms of contraception while on the study and for 2 days after last dose of acelabrutinib or 90 days after the last dose of ibrutinib, which
•Known central nervous system (CNS) lymphoma or leukemia.
•Known prolymphocytic leukemia or history of, or currently suspected, Richter’s syndrome.
•Uncontrolled autoimmune hemolytic anemia (AIHA) or idiopathic thrombocytopenic purpura (ITP) defined as declining hemoglobin or platelet count secondary to autoimmune destruction within the screening period or requirement for high doses of steroids (> 20 mg daily of prednisone daily or equivalent).
•Prior exposure to ibrutinib or to a B-cell receptor (BCR) inhibitor (eg, Bruton tyrosine kinase [Btk] inhibitors or phosphoinositide-3 [PI3] kinase inhibitors or Syk inhibitors) or a BCL-2 inhibitor (eg, ABT-199).
•Received any chemotherapy, external beam radiation therapy, anticancer antibodies, or investigational drug within 30 days before first dose of study drug.
•Corticosteroid use > 20 mg within 1 week before first dose of study drug, except as indicated for other medical conditions such as inhaled steroid for asthma, topical steroid use, or as premedication for administration of study drug or contrast. For example, subjects requiring steroids at daily doses > 20 mg prednisone equivalent systemic exposure daily, or those who are administered steroids for leukemia control or white blood cell count lowering are excluded.
•Prior radio- or toxin-conjugated antibody therapy.
•Prior allogeneic stem cell transplant or autologous transplant.
•Major surgery within 4 weeks before first dose of study drug.
•History of prior malignancy except for the following:
oMalignancy treated with curative intent and with no evidence of active disease present for more than 3 years before Screening and felt to be at low risk for recurrence by treating physician
oAdequately treated lentigo maligna melanoma without current evidence of disease or adequately controlled non-melanomatous skin cancer
oAdequately treated cervical carcinoma in situ without current evidence of disease
•Significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, or myocardial infarction within 6 months of screening, or any Class 3 or 4 cardiac disease as defined by the New York Heart Association Functional Classification, or QTc > 480 msec at screening.
•Unable to swallow capsules or malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel or gastric bypass, symptomatic inflammatory bowel disease, or partial or complete bowel obstruction.
•Uncontrolled active systemic fungal, bacterial, viral, or other infection (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment) or ongoing intravenous anti-infective treatment.
•Known history of infection with human immunodeficiency virus (HIV).
•Serologic status reflecting active hepatitis B or C infection. Subjects with hepatitis B core antibody positive who are surface antigen negative or who are hepatitis C antibody positive will need to have a negative polymerase chain reaction (PCR) result before randomization. Those who are hepatitis B surface antigen positive or hepatitis B PCR positive and those who are hepatitis C PCR positive will be excluded.
•History of stroke or intracranial hemorrhage within 6 months before randomization.
•History of bleeding diathesis (eg, hemophilia, von Willebrand disease).
•Requires or receiving anticoagulation with warfarin or equivalent vitamin K antagonis
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method