B-Cell Chronic Lymphocytic Leukemia
Conditions
Keywords
B-Cell Chronic Lymphocytic Leukemia, Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, Marginal Zone Lymphoma, Mantle Cell Lymphoma, Follicular Lymphoma, Waldenstrom's Macroglobulinemia, Ibrutinib, IMBRUVICA, PCI-32765, JNJ-54179060
Brief summary
The purpose of this study is to assess the effect of a moderate Cytochrome P450 (CYP) 3A inhibitor (erythromycin) and a strong CYP3A inhibitor (voriconazole) on the steady-state pharmacokinetics (PK \[the study of the way a drug enters and leaves the blood and tissues over time\]) of repeated oral doses of ibrutinib in participants with B-cell malignancy (cancer or other progressively enlarging and spreading tumors).
Detailed description
This is an open-label (participants and researchers are aware about the treatment participants are receiving), multi-center (when more than 1 hospital or medical school team work on a medical research study), drug-drug interaction (DDI) study of ibrutinib with the moderate and the strong CYP3A inhibitors (erythromycin and voriconazole respectively) in participants with B-cell malignancies (including Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma \[CLL/SLL\], Follicular Lymphoma \[FL\], Marginal Zone Lymphoma \[MZL\], Waldenstrom's Macroglobulinemia \[WM\] or Mantle Cell Lymphoma \[MCL\]). The study will consist of a Screening Phase (28 days), a Treatment Phase (consisting of six 28-days cycles), and an End-of-Treatment (EoT) Visit (within 30 days after the last dose of study drug). The study will consist of 2 Parts. In Part 1, extent of the DDI between ibrutinib at dose level of 140 milligram (mg) and CYP3A inhibitors will be assessed. After completion of Part 1 of the study, an interim analysis of all available PK and safety data will be conducted and Part 2 will only be performed if the observed drug interaction is less than anticipated based on current information. In Part 2, safety and PK of ibrutinib at dose level of 560 mg administered with CYP3A inhibitors will be assessed. Participants who continue to derive clinical benefit from ibrutinib treatment at the end of this study, and who are eligible to continue in the PCI-32765CAN3001 study (NCT01804686) will end their participation in this trial, have an EoT visit completed, and will continue receiving ibrutinib as a part of the PCI-32765CAN3001 protocol. Participants' safety will be monitored throughout the study.
Interventions
DRUGIbrutinib
Ibrutinib capsule (at dose level of 140 or 420 or 560 mg) will be taken orally QD up to six, 28-days cycles.
DRUGErythromycin
Erythromycin 500 mg tablet will be taken orally TID (Part1 Cycle 1: on Days 5-10 and morning dose on Day 11; Part2 Cycle 1: on Days 5-17 and morning dose on Day 18).
DRUGVoriconazole
Voriconazole 200 mg tablet will be taken orally BD (Part1 Cycle 1: on Days 19-25; Part2 Cycle 1: on Days 5-17).
Sponsors
Janssen Research & Development, LLC
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically or cytologically confirmed Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma (CLL/SLL), Marginal Zone Lymphoma (MZL), Mantle Cell Lymphoma (MCL), Follicular Lymphoma (FL), or Waldenstrom's Macroglobulinemia (WM) * Relapsed or refractory disease after at least 1 prior line of systemic therapy (participants with FL or MZL must have failed anti-CD20 monoclonal antibody containing chemotherapy regimen) * Eastern Cooperative Oncology Group Performance Status score of 0 or 1 * Hematology values within the following limits: a) Absolute neutrophil count (ANC) greater than and equal to (\>=) 1.0\*10\^9 per liter (L); b) Platelets \>=50\*10\^9/L without transfusion support within 7 days; c) Hemoglobin \>=8 gram per deciliter (g/dL) without transfusion support within 7 days; d) Prothrombin time /International normalized ratio (PT/INR) less than equal to (\<=) 1.5\*Upper Limit of Normal (ULN) and activated partial thromboplastin time (aPTT) \<=1.5\*ULN * Biochemical values within the following limits: a) Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \<=3.0\*ULN; b) Total bilirubin \<=1.5\*ULN (unless due to Gilbert's syndrome); c) Serum creatinine \<=1.5\*ULN or a calculated creatinine clearance of \>=50 milliliter per minute per 1.73 square meter
Exclusion criteria
* Major surgery within 4 weeks of the first dose of ibrutinib * Diagnosed or treated for malignancy other than the indication under study except for: a) Adequately treated non-melanoma skin cancer or lentigo maligna, curatively treated in-situ cancer without evidence of disease; b) Malignancy treated with curative intent and with no known active disease present for \>=3 years before the first dose of ibrutinib * History of stroke or intracranial hemorrhage within 6 months prior to the first dose of ibrutinib * History of galactose intolerance * Requires anticoagulation with warfarin or equivalent vitamin K antagonists (for example, phenprocoumon)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Minimum Observed Plasma Concentration (Cmin) of Ibrutinib | Cycle 1: 0 hour (hr) pre-dose on Day 1; 0 hr pre-dose, 0.5,1,2,3,4,6,8 and 24 hrs post-dose on Day 4, 11, 18, and 25 | The Cmin is the minimum observed plasma concentration. |
| Area Under the Plasma Concentration-Time Curve From Time Zero to 24 Hours (AUC[0-24]) of Ibrutinib | Cycle 1: 0 hr pre-dose, 0.5,1,2,3,4,6,8 and 24 hrs post-dose on Day 4, 11, 18, and 25 | The AUC (0-24) is the area under the plasma concentration-time curve from time zero to 24 hours. |
| Metabolite to Parent (M/P) Ratio of Ibrutinib | Cycle 1: 0 hour (hr) pre-dose on Day 1; 0 hr pre-dose, 0.5,1,2,3,4,6,8 and 24 hrs post-dose on Day 4, 11, 18, and 25 | Ratio of ibrutinib metabolite concentration to parent compound (ibrutinib) concentration will be assessed. |
| Maximum Observed Plasma Concentration (Cmax) of Ibrutinib | Cycle 1: 0 hour (hr) pre-dose on Day 1; 0 hr pre-dose, 0.5,1,2,3,4,6,8 and 24 hrs post-dose on Day 4, 11, 18, and 25 | The Cmax is the maximum observed plasma concentration. |
| Time to Reach Maximum Observed Plasma Concentration (Tmax) of Ibrutinib | Cycle 1: 0 hour (hr) pre-dose on Day 1; 0 hr pre-dose, 0.5,1,2,3,4,6,8 and 24 hrs post-dose on Day 4, 11, 18, and 25 | The Tmax is defined as actual sampling time to reach maximum observed analyte concentration. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) | Screening up to end of study (up to 8 months) | An AE is any untoward medical occurrence in a participant participating in a clinical study that does not necessarily have a causal relationship with the pharmaceutical/biological agent under study. An SAE is any AE that results in: death, persistent or significant disability/incapacity, requires inpatient hospitalization or prolongation of existing hospitalization, is life-threatening experience, is a congenital anomaly/birth defect and may jeopardize participant and/or may require medical or surgical intervention to prevent one of the outcomes listed above. |
| Partial Area Under the Plasma Concentration-Time Curve Between 2 Defined Timepoints (AUC [t1 and t2]) of Voriconazole | Cycle 1: 0 hour (hr) pre-dose on Day 5; 0 hr pre-dose, 0.5,1,2,3,4,6 and 24 hrs post-dose on Day 18 and 25 | The AUC (t1 and t2) is the partial area under the plasma concentration-time curve from time 't1' to 't2' hours. |
Countries
Canada, Russia, Spain
Outcome results
None listed