- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT02537613
재발성 또는 불응성 만성 림프 구성 백혈병 환자에서 Ibrutinib + Obinutuzumab에 대한 연구
재발성 또는 불응성 만성 림프구성 백혈병 환자에서 이브루티닙과 오비누투주맙을 병용한 Ib상 연구
This research study is evaluating a combination of two drugs, ibrutinib and obinutuzumab, as a possible treatment for Chronic Lymphocytic Leukemia (CLL).
연구 개요
상세 설명
This research study is a Phase I clinical trial, which tests the safety of an investigational intervention and also tries to define the best order of administration of these two drugs. "Investigational" means that the intervention is being studied. The FDA (the U.S. Food and Drug Administration) has approved ibrutinib and obinutuzumab individually for the treatment of patients with Chronic Lymphocytic Leukemia, your type of cancer. However, the FDA has not approved the combination of these two drugs as a treatment for any disease.
Ibrutinib is a type of drug called a kinase inhibitor. It is believed to block a type of protein called a kinase that helps leukemia cells live and grow. By blocking this, it is possible that the study drug will kill cancer cells or stop them from growing.
Obinutuzumab is a type of drug called a monoclonal antibody. It is believed to attach to a protein called CD20 on the outside of a Chronic Lymphocytic Leukemia cell. By attaching to the cell, the antibody can cause the Chronic Lymphocytic Leukemia cell to die.
In this research study, the investigators are assessing the safety of various dosing regimens of ibrutinib and obinutuzumab. The investigators are trying to determine whether it is better to give one drug before the other or if they can be started at the same time.
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
연구 장소
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Massachusetts
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Boston, Massachusetts, 미국, 02114
- Massachusetts General Hospital
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Boston, Massachusetts, 미국, 02215
- Dana Farber Cancer Institute
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New York
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Rochester, New York, 미국, 14642
- University of Rochester Wilmot Cancer Inst.
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North Carolina
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Durham, North Carolina, 미국, 27710
- Duke University Medical Center
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion criteria:
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Must have a confirmed diagnosis of Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma as per IW-CLL 2008 criteria and require therapy based on meeting at least one of the following criteria:
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Evidence of progressive marrow failure with anemia (hemoglobin <11.0 g/L) and/or thrombocytopenia (platelets <100 x 10^9/L)
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Massive (≥6 cm below the left costal margin), progressive, or symptomatic splenomegaly
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Massive nodes (at least 10 cm longest diameter), progressive, or symptomatic lymphadenopathy
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Progressive lymphocytosis with an increase of more than 50% over a 2-month period or LDT of <6 months.
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Autoimmune anemia and/or thrombocytopenia that is poorly responsive to corticosteroids
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Constitutional symptoms, defined as 1 or more of the following:
- unintentional weight loss >10% within 6 months prior to screening
- significant fatigue (inability to work or perform usual activities) fevers >100.5° F or 38.0° C for 2 or more weeks prior to screening without evidence of infection
- night sweats for more than 1 month prior to screening without evidence of infection
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Relapsed after or refractory to at least one prior Chronic Lymphocytic Leukemia-directed therapy
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Age greater than or equal to 18 years
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ECOG Performance Status <2
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Heme criteria at screening, unless significant bone marrow involvement of Chronic Lymphocytic Leukemia confirmed on biopsy:
- Absolute Neutrophil Count (ANC) ≥500 cells/mm3 (0.5 x 10^9/L). Growth factor allowed to achieve
- Platelet count ≥25,000 cells/mm3 (25 x 10^9/L) independent of transfusion within 7 days of screening
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Adequate hepatic function defined as: AST and ALT ≤ 4.0 x upper limit of normal (ULN), bilirubin ≤2.0 x upper limit of normal (ULN) unless bilirubin rise is due to Gilbert's syndrome)
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Adequate renal function defined by serum creatinine <2.0 x upper limit of normal (ULN) unless due to biopsy proven Chronic Lymphocytic Leukemia kidney infiltration
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Women of child-bearing potential and men must agree to use adequate contraception
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Patients who have undergone prior allo transplant are eligible provided that their transplant day 0 is > 6 months from their first dose of study drug
Exclusion Criteria:
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History of severe allergic or anaphylactic reactions to monoclonal antibody therapy
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Prior treatment with either obinutuzumab or ibrutinib
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History of other malignancies, except:
- Malignancy treated with curative intent and with no known active disease present for ≥3 years before the first dose of study drug and felt to be at low risk for recurrence by treating physician.
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.
- Adequately treated carcinoma in situ without evidence of disease.
- Low-risk prostate cancer on active surveillance
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Concurrent systemic immunosuppressant therapy (eg, cyclosporine A, tacrolimus, etc., or chronic administration of >20 mg/day of prednisone) within 28 days of the first dose of study drug.
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Vaccinated with live, attenuated vaccines within 4 weeks of first dose of study drug.
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Recent infection requiring systemic treatment that was completed ≤7 days before the first dose of study drug.
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Known bleeding disorders or hemophilia.
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History of stroke or intracranial hemorrhage within 6 months prior to enrollment.
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Known history of HIV or active hepatitis C virus (HCV) or hepatitis B virus (HBV).
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Any uncontrolled active systemic infection.
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Major surgery within 4 weeks of first dose of study drug.
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Currently active, clinically significant cardiovascular disease, such as uncontrolled arrhythmia or Class 3 or 4 CHF as defined by the NYHA Functional Classification; or a history of Myocardial Infarction, unstable angina, or acute coronary syndrome within 6 months prior to randomization.
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Lactating or pregnant.
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Patients receiving any other study agents
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Patients with known Central Nervous System involvement
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Baseline QT Interval Corrected by the Fridericia Correction Formula (QTcF) >480 ms unless Left Bundle Branch Block
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Patients who require warfarin or other vitamin K antagonists for anticoagulation
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Concurrent administration of strong inhibitors or inducers of CYP3A
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Arm A- obinutuzumab -> ibrutinib
Participants enrolled in Arm A will receive obinutuzumab weekly starting cycle 1, and will receive obinutuzumab monthly during cycles 2-6. Participants will begin to take ibrutinib daily starting cycle 2 and will continue with daily ibrutinib until the end of treatment. |
Obinutuzumab given weekly during cycle 1, then monthly during cycles 2-6
다른 이름들:
Ibrutinib given once daily by mouth
다른 이름들:
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실험적: Arm B- ibrutinib -> obinutuzumab
Participants enrolled in Arm B will begin to take ibrutinib daily starting cycle 1 and will continue with daily ibrutinib until the end of treatment. Participants will begin to receive obinutuzumab weekly starting cycle 2, and will receive obinutuzumab monthly during cycles 3-7 |
Obinutuzumab given weekly during cycle 1, then monthly during cycles 2-6
다른 이름들:
Ibrutinib given once daily by mouth
다른 이름들:
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실험적: Arm C- obinutuzumab/ibrutinib
Participants enrolled in Arm C will begin to take ibrutinib daily starting cycle 1 and will continue with daily ibrutinib until the end of treatment. At the same time, participants will begin to receive obinutuzumab weekly starting cycle 1, and will receive obinutuzumab monthly during cycles 2-6. |
Obinutuzumab given weekly during cycle 1, then monthly during cycles 2-6
다른 이름들:
Ibrutinib given once daily by mouth
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Grade 3-5 Treatment-related Toxicity Rate
기간: AE evaluated at cycle 1 day day 1, 2, 8 and 15; cycle 2 day 1, 8, 15 and 22; then each cycle day 1 until end of treatment.
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All grade 3-5 adverse events (AE) with treatment attribution of possibly, probably or definite based on CTCAEv4 that are not resolved in accordance with treatment guidelines were counted. Rate is the proportion of treated participants experiencing at least one of these adverse events as defined during the time of observation. |
AE evaluated at cycle 1 day day 1, 2, 8 and 15; cycle 2 day 1, 8, 15 and 22; then each cycle day 1 until end of treatment.
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Overall Response Rate (ORR)
기간: Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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The overall response rate (ORR) was defined as the proportion of participants achieving complete response (CR) or partial response (PR) based on Chronic Lymphocytic Leukemia (IW-CLL) criteria. |
Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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Partial Response Rate (PRR)
기간: Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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The PRR was defined as the proportion of participants achieving partial response (PR) based on Chronic Lymphocytic Leukemia (IW-CLL) criteria. |
Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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Complete Response Rate (CRR)
기간: Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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The CRR was defined as the proportion of participants achieving complete response (CR) based on Chronic Lymphocytic Leukemia (IW-CLL) criteria. |
Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD). Median (range) duration of treatment is 29.9 (range 0.5, 98.1) months.
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Minimal Residual Disease (MRD) Rate
기간: Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD).
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MRD rate was defined as the proportion of participants achieving MRD in bone marrow |
Disease screening at baseline, cycle 3-7 at day one and end of treatment or disease progression (PD).
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Median Progression-Free Survival (PFS)
기간: Through final follow-up visit (up to 9.63 years).
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Progression-free survival based on the Kaplan-Meier method is defined as the duration between randomization and documented disease progression (PD) or death, or is censored at time of last dsease assessment. |
Through final follow-up visit (up to 9.63 years).
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공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Matthew Davids, MD, MMSc, Dana-Farber Cancer Institute
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정된)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
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