A Trial to See the Effects of ACP-196 (the test drug) in Patients who have Mantle Cell Lymphoma
- Conditions
- Mantle Cell LymphomaMedDRA version: 20.0Level: HLTClassification code: 10026798Term: Mantle cell lymphomas Class: 10029104Therapeutic area: Diseases [C] - Neoplasms [C04]
- Registration Number
- CTIS2023-509352-34-00
- Lead Sponsor
- Acerta Pharma B.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Men and women = 18 years of age., Willing and able to participate in all required evaluations and procedures in this study protocol including swallowing capsules or tablets without difficulty., Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (in accordance with national and local patient privacy regulations)., Pathologically confirmed MCL, with documentation of monoclonal B cells that have a chromosome translocation t(11;14)(q13;q32) and/or overexpress cyclin D1., Disease has relapsed after or been refractory to = 1 prior therapy for MCL and now requires further treatment., Documented failure to achieve at least PR with, or documented disease progression after, the most recent treatment regimen., Presence of radiographically measurable lymphadenopathy or extranodal lymphoid malignancy (defined as the presence of = 1 lesion that measures = 2.0 cm in the longest dimension and = 1.0 cm in the longest perpendicular dimension as assessed by computed tomography [CT] scan)., At least 1, but no more than 5, prior treatment regimens for MCL (Note: Subjects having received = 2 cycles of prior treatment with bortezomib or any other commercially available proteasome inhibitor, either as a single agent or as part of a combination therapy regimen, will be considered to be proteasome inhibitor-exposed.), Eastern Cooperative Oncology Group (ECOG) performance status of = 2., Women who are sexually active and can bear children must agree to use highly effective forms of contraception during the study and for 2 days after the last dose of study drug., This criterion has been removed as of protocol amendment 8.
Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer from which the subject has been disease free for = 2 years or which will not limit survival to < 2 years. Note: these cases must be discussed with the medical monitor., Known history of human immunodeficiency virus (HIV) or active infection with hepatitis C virus (HCV) or hepatitis B virus (HBV) or any uncontrolled active systemic infection., Major surgery within 4 weeks before first dose of study drug., Uncontrolled autoimmune hemolytic anemia or idiopathic thrombocytopenia purpura., Known history of a bleeding diathesis (eg, hemophilia, von Willebrand disease), History of stroke or intracranial hemorrhage within 6 months before the first dose of study drug., Requires or receiving anticoagulation with warfarin or equivalent vitamin K antagonist (eg, phenprocoumon) within 7 days of first dose of study drug., Requires treatment with proton pump inhibitors (eg, omeprazole, esomeprazole, lansoprazole, exlansoprazole, rabeprazole, or pantoprazole). Note: this criterion no longer applies to patients who have switched from acalabrutinib capsules to tablets., ANC < 0.75 x 109/L or platelet count < 50 x 109/L; for subjects with disease involvement in the bone marrow, ANC < 0.50 x 109/L or platelet count < 30 x 109/L., Creatinine > 2.5 x institutional upper limit of normal (ULN); total bilirubin > 2.5 x ULN ; and aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3.0 x ULN., Breastfeeding or pregnant., A life-threatening illness, medical condition or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, interfere with the absorption or metabolism of ACP-196, or put the study outcomes at undue risk., Concurrent participation in another therapeutic clinical trial., Known central nervous system (CNS) lymphoma or leptomeningeal disease., Requires treatment with a strong CYP3A inhibitor/inducer., Presence of a gastrointestinal ulcer diagnosed by endoscopy within 3 months prior to screening., 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 corrected QT interval (QTc) > 480 msec., Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel, gastric bypass, symptomatic inflammatory bowel disease, or partial or complete bowel obstruction., Any immunotherapy within 4 weeks of first dose of study drug., The time from the last dose of the most recent chemotherapy or experimental therapy to the first dose of study drug is < 5 times the half-life of the previously administered agent(s)., Prior exposure to a BCR inhibitor (eg, BTK, phosphoinositide-3 kinase (PI3K), or SYK inhibitors) or BCL-2 inhibitor (eg, ABT-199)., Ongoing immunosuppressive therapy, including systemic or enteric corticosteroids for treatment of MCL or other conditions. Note: Subjects may use topical or inhaled corticosteroids or low-dose steroids (= 10 mg of prednisone or equivalent per day) as therapy for comorbid conditions. During study participation, subjects may also receive systemic or enteric corticosteroids as needed for treatment-emergent comorbid conditions., Grade = 2 toxicity (other than alopecia
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: To determine the activity of acalabrutinib in subjects with relapsed/refractory (R/R) MCL as measured primarily by response rate.<br>In addition, activity of acalabrutinib will be assessed by duration of response, progression-free survival, and overall survival.;Secondary Objective: To characterize the safety profile of acalabrutinib, To characterize the pharmacokinetic (PK) profile of acalabrutinib, To evaluate the PD effects of acalabrutinib;Primary end point(s): The primary endpoint of the study is the overall response rate (ORR), defined as the proportion of subjects achieving either a partial response (PR) or complete response (CR) according to the Lugano Classification for NHL as assessed by investigators.
- Secondary Outcome Measures
Name Time Method Secondary end point(s):Efficacy: • duration of response (DOR) • progression-free survival (PFS) • overall survival (OS) • IRC-assessed ORR, DOR and PFS per Lugano Classification;Secondary end point(s):Safety: • frequency and severity of adverse events • frequency of adverse events requiring discontinuation of study drug or dose reductions • effect of acalabrutinib on peripheral T/B/natural killer (NK) cell counts • effect of acalabrutinib on serum immunoglobulin levels;Secondary end point(s):Pharmacokinetics: • plasma pharmacokinetics of acalabrutinib