- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01164709
Nelfinavir Mesylate and Bortezomib in Treating Patients With Relapsed or Progressive Advanced Hematologic Cancer
Phase I Trial of Nelfinavir and Bortezomib in Advanced Hematologic Malignancies
RATIONALE: Nelfinavir mesylate and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Bortezomib may also stop the growth of hematologic cancer by blocking blood flow to the cancer. Giving nelfinavir mesylate together with bortezomib may kill more cancer cells.
PURPOSE: This phase I trial is studying the side effects and best dose of nelfinavir mesylate when given together with bortezomib in treating patients with relapsed or progressive advanced hematologic cancer.
연구 개요
상태
상세 설명
OBJECTIVES:
- To assess the safety of nelfinavir mesylate in combination with bortezomib in patients with relapsed or progressive, advanced hematologic malignancies.
- To establish the phase II recommended dose of nelfinavir mesylate in these patients.
OUTLINE: This is a multicenter, dose-escalation study of nelfinavir mesylate.
Patients receive oral nelfinavir mesylate twice daily on days 1-21 and bortezomib IV on days 8, 11, 15, and 18 in course 1. Course 1 has a duration of 28 days. Beginning in course 2, patients receive oral nelfinavir mesylate twice daily on days 1-14 and bortezomib IV on days 1, 4, 8, and 11. Treatment repeats every 21 days for 2 courses. Patients with responding disease may continue to receive nelfinavir mesylate and bortezomib for up to 4 additional courses.
After completion of study treatment, patients are followed for 30 days.
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
연구 장소
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Bern, 스위스, CH-3010
- Inselspital Bern
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Chur, 스위스, CH-7000
- Kantonsspital Graubuenden
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Lausanne, 스위스, CH-1011
- Centre hospitalier universitaire vaudois
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St. Gallen, 스위스, CH-9007
- Kantonsspital - St. Gallen
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
DISEASE CHARACTERISTICS:
Diagnosed with advanced hematologic malignancies meeting the following criteria:
Multiple myeloma
- Received ≥ 2 lines of prior chemotherapy (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
- Acute myeloid leukemia
- Acute lymphoblastic leukemia
- Diffuse large B-cell lymphoma
- Hodgkin lymphoma
- Mantle cell lymphoma
Mature T- and NK-cell neoplasms restricted to the following WHO-defined entities:
- T-cell prolymphocytic leukemia
- T-cell large granular lymphocytic leukemia
- Aggressive NK-cell leukemia
- Adult T-cell leukemia/lymphoma
- Extranodal NK/T-cell lymphoma (nasal type)
- Mycosis fungoides
- Sézary syndrome
- Primary CD30-positive T-cell lymphoproliferative disorders
- Primary cutaneous anaplastic large cell lymphoma
- Primary cutaneous gamma-delta T-cell lymphoma
- Peripheral T-cell lymphoma (not otherwise specified)
- Angioimmunoblastic T-cell lymphoma
- Anaplastic large cell lymphoma (ALK-positive/ALK-negative)
- Grade 3B follicular lymphoma
- Relapsed following or progressed during standard therapy
Meeting the following criteria:
- Standard intensive therapy is not feasible
- Current disease state for which there is no standard effective therapy
- Refused standard therapy where no curative option exists
Measurable disease, defined as the following:
- Myeloma: measurable serum monoclonal protein > 1 g/dL for IgG, or > 0.5 g/dL for IgA, IgM or IgD, or difference between involved and uninvolved free light chain levels in serum > 100 mg/L
- Lymphoma: must have ≥ 1 lesion measurable by CT (longest diameter ≥ 15 mm)
- Acute leukemia: ≥ 20% blasts in bone marrow or in peripheral blood (≥ 200/mL blasts in peripheral blood)
- No HIV-associated lymphoma
PATIENT CHARACTERISTICS:
- WHO performance status 0-2
- Absolute neutrophil count ≥ 1,500/mm³
- Platelet count ≥ 75,000/mm³ (if bone marrow impairment, ≥ 20,000/mm^3)
- Hemoglobin > 80 g/L (if considered to be caused by the underlying hematologic malignancy or bone marrow impairment, > 80 g/L after transfusion)
- Bilirubin ≤ 1.5 times upper limit of normal (ULN) (if suspected hemolysis, direct bilirubin ≤ 1.5 times ULN)
- ALT ≤ 2.5 times ULN
- Calculated creatinine clearance > 30 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 12 months after completion of study treatment
- Willing and capable to comply with an oral regimen
- Capable of understanding information given by the investigator on the trial
- Able to adhere and remain in geographic proximity to allow proper staging, treatment, and followup
- No other non-hematologic malignancy within the past 5 years, except adequately treated cervical carcinoma in situ or localized nonmelanoma skin cancer
- No known chronic hepatitis B or C infection or known HIV infection
No serious underlying medical condition (at the judgment of the investigator) which would impair the ability of the patient to participate in the trial, including any of the following:
- Active autoimmune disease
- Uncontrolled diabetes
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Cardiac arrhythmia
- Psychiatric disorder
- No myocardial infarction within the past 6 months
- No polyneuropathy > grade 1 significantly interfering with activities of daily living or painful polyneuropathy
- No known hypersensitivity to trial drugs or hypersensitivity to any other component of the trial drugs
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No more than 4 prior lines of chemotherapeutic regimens (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
- More than 30 days since prior treatment in a clinical trial
More than 30 days since prior and no concurrent chemotherapy or biologic agents
- For patients with acute leukemia, hydroxyurea may be given up to 48 hours before first administration of the trial treatment, and low dose cytarabine (up to 20 mg/m^2) and mitoxantrone up to 20 mg up to 14 days before first dosing
- At least 1 week since prior and no concurrent CYP3A4 modulators
- No concurrent other experimental drugs
- No concurrent radiotherapy
- No concurrent antineoplastic therapy with chemotherapeutic or biologic agents
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: bortezomib + nelfinavir
escalation 3 by 3 cohorts
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Bortezomib i.v., day 8, 11, 15, 18; 1.3 mg/m2
다른 이름들:
p.o., days 1 to 21; dose level: (625), 1250, 1875, or 2500 mg, 2x/d
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Dose limiting toxicity
기간: during first cycle
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during first cycle
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Objective response
기간: during treatment
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during treatment
|
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Adverse events according to NCI CTCAE v.4.0
기간: during treatment + 30 days
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during treatment + 30 days
|
공동 작업자 및 조사자
수사관
- 연구 의자: Christoph Driessen, MD, Cantonal Hospital of St. Gallen
- 수석 연구원: Dagmar Hess, MD, Cantonal Hospital of St. Gallen
- 수석 연구원: Roger von Moos, MD, Kantonsspital Graubuenden
- 수석 연구원: Thomas Pabst, MD, University Hospital Inselspital, Berne
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
- 3기 성인 미만성 대세포 림프종
- IV기 3등급 여포성 림프종
- IV기 성인 미만성 대세포 림프종
- 재발성 등급 3 여포성 림프종
- 재발성 성인 미만성 대세포 림프종
- 11q23(MLL) 이상이 있는 성인 급성 골수성 백혈병
- inv(16)(p13;q22)가 있는 성인 급성 골수성 백혈병
- t(15;17)(q22;q12)가 있는 성인 급성 골수성 백혈병
- t(16;16)(p13;q22)가 있는 성인 급성 골수성 백혈병
- t(8;21)(q22;q22)가 있는 성인 급성 골수성 백혈병
- 속발성 급성 골수성 백혈병
- 재발성 성인 급성 골수성 백혈병
- 재발성 성인 호지킨 림프종
- 3기 3등급 여포성 림프종
- 3기 맨틀 세포 림프종
- IV기 맨틀 세포 림프종
- 재발성 맨틀 세포 림프종
- 3기 성인 호지킨 림프종
- IV기 성인 호지킨 림프종
- 3기 피부 T 세포 비호지킨 림프종
- IV기 피부 T 세포 비호지킨 림프종
- 재발 성 피부 T 세포 비호 지킨 림프종
- 3기 성인 T세포 백혈병/림프종
- 4기 성인 T세포 백혈병/림프종
- 재발성 성인 T 세포 백혈병/림프종
- 혈관면역모세포성 T세포 림프종
- 역형성 대세포 림프종
- III기 균상 식육종/세자리 증후군
- IV기 균상 식육종/세자리 증후군
- 재발성 균상 식육종/세자리 증후군
- 성인 비강형 림프절외 NK/T 세포 림프종
- 불응성 다발성 골수종
- 재발성 성인 급성 림프구성 백혈병
- 전림프구성 백혈병
- 말초 T 세포 림프종
- T 세포 거대 과립 림프구 백혈병
- aggressive NK-cell leukemia
추가 관련 MeSH 약관
기타 연구 ID 번호
- SAKK 65/08
- SWS-SAKK-65/08
- EU-21051
- SWS-SAKK-JC26866138LYM1005
- CDR0000681442 (레지스트리 식별자: CDR0000681442)
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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