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

Phase 1

Recruiting

• Conditions: High Risk Chronic Lymphocytic Leukaemia; MedDRA version: 21.0Level: LLTClassification code: 10008976Term: Chronic lymphocytic leukemia Class: 10029104; Therapeutic area: Diseases [C] - Neoplasms [C04]

• Registration Number: CTIS2023-509347-27-00
• Lead Sponsor: Acerta Pharma B.V.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-03-26
• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

Men and women = 18 years of age., Men who are sexually active and can beget children must agree to use highly effective forms of contraception during the study and for 2 days after the last dose of acalabrutinib or 90 days after the last dose of ibrutinib, whichever is longer., Men must agree to refrain from sperm donation during the study and for 2 days after the last dose of acalabrutinib or 90 days after the last dose of ibrutinib, whichever is longer., Must be willing and able to adhere to the study visit schedule, understand and comply with other protocol requirements, and provide written informed consent and authorization to use protected health information (in accordance with national and local patient privacy regulations). Note vulnerable subjects, as defined in the International Conference on Harmonisation (ICH) GCP, are not allowed on this protocol (eg, prisoners or institutionalized subjects)., ECOG performance status of 0 to 2., Diagnosis of CLL that meets published diagnostic criteria (Hallek 2008): a. Monoclonal B-cells (either kappa or lambda light chain restricted) that are clonally co-expressing = 1 B-cell marker (CD19, CD20, or CD23) and CD5. b. Prolymphocytes may comprise = 55% of blood lymphocytes. c. Presence of = 5 x 109 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: a. Presence of 17p del by central laboratory. b. Presence of 11q del by central laboratory., Active disease meeting = 1 of the following IWCLL 2008 criteria for requiring treatment: a. 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). b. Massive (ie, = 6 cm below the left costal margin), progressive, or symptomatic splenomegaly. c. Massive nodes (ie, = 10 cm in the longest diameter), progressive, or symptomatic lymphadenopathy. d. Progressive lymphocytosis with an increase of > 50% over a 2-month period or a LDT of < 6 months. LDT may be obtained by linear regression extrapolation of 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 109/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. e. Autoimmune anemia and/or thrombocytopenia that is poorly responsive to standard therapy. f. Constitutional symptoms documented in the subject’s chart with supportive objective measures, as appropriate, defined as = 1 of the following disease-related symptoms or signs: i. Unintentional weight loss = 10% within the previous 6 months before Screening. ii. Significant fatigue (ie, ECOG performance status 2 or worse; inability to work or perform usual activities). iii. Fevers > 100.5°F or 38.0°C for = 2 weeks before Screening without evidence of infection. iv. Night sweats for > 1 month before Screening without evidence of infection., Must have received = 1 prior therapies for CLL., Meet the following laboratory parameters: a. ANC = 750 cells/µL (0.75 x 109/L) or = 500 cells/µL (0.50 x 109/L) in subjects with documented bone marrow involvement, and independent of growth factor support 7 days before assessment. b. Platelet count = 30,000 cells/µL (30 x 109/L) without transfus

Exclusion Criteria

Subjects will be ineligible for this study if they meet any of the following criteria: - Known CNS lymphoma or leukemia., History of prior malignancy except: a. Malignancy 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. b. Adequately treated lentigo malign melanoma without current evidence of disease or adequately controlled non-melanomatous skin cancer c. Adequately 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 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 antagonists (eg, phenprocoumon) within 7 days of first dose of study drug., Requires treatment with a strong CYP3A inhibitor/inducer., Known prolymphocytic leukemia or history of, or currently suspected, Richter’s syndrome., Requires treatment with proton-pump inhibitors (eg, omeprazole, esomeprazole, lansoprazole, dexlansoprazole, rabeprazole, or pantoprazole)., Breastfeeding or pregnant., Concurrent participation in another therapeutic clinical trial., Presence of a gastrointestinal ulcer diagnosed by endoscopy within 3 months before screening., Uncontrolled AIHA or 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 BCR inhibitor (eg Btk or PI3 kinase 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 equivale

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified