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A Study of ABT-263 in Subjects With Relapsed or Refractory Lymphoid Malignancies

2021년 7월 28일 업데이트: AbbVie (prior sponsor, Abbott)

A Phase 1/2a Study Evaluating the Safety, Pharmacokinetics and Efficacy of ABT-263 in Subjects With Relapsed or Refractory Lymphoid Malignancies

The Phase 1 portion of the study evaluated the pharmacokinetic profile and safety of ABT-263 with the objective of defining the dose limiting toxicity and maximum tolerated dose in subjects with lymphoid malignancies. The Phase 2a portion of the study is evaluating ABT-263 using a step-up dosing regimen and may be increased to the defined recommended Phase 2 dose to obtain additional safety information and a preliminary assessment of efficacy in subject with lymphoid malignancies. The Extension portion of the study is to allow Phase 2a subjects who remain active 1 year after the last subject enrolls or who have been on study approximately 1 year to continue receiving ABT-263 with less frequent study evaluations. Subjects in the Extension Study will continue receiving study drug for up to 7 years after the last subject transitions to the Extension Study, or until disease progression or toxicity that necessitates discontinuation (whichever comes first).

연구 개요

상세 설명

Enrollment breakdown: Entered Study: Phase 1a: 39; Phase 1b: 19; Phase 2a: 33; Total: 91 Entered Treatment: Phase 1a: 38; Phase 1b: 17; Phase 2a: 26; Total: 81

연구 유형

중재적

등록 (실제)

81

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • California
      • Los Angeles, California, 미국, 90033
        • Site Reference ID/Investigator# 4997
      • Los Angeles, California, 미국, 90095
        • Site Reference ID/Investigator# 9104
    • Maryland
      • Bethesda, Maryland, 미국, 20892
        • Site Reference ID/Investigator# 2613
    • Massachusetts
      • Boston, Massachusetts, 미국, 02215
        • Site Reference ID/Investigator# 40243
      • Boston, Massachusetts, 미국, 02215
        • Site Reference ID/Investigator# 4745
    • New York
      • Buffalo, New York, 미국, 14263
        • Site Reference ID/Investigator# 2628
      • New York, New York, 미국, 10016
        • Site Reference ID/Investigator# 23543
      • New York, New York, 미국, 10021
        • Site Reference ID/Investigator# 2627
      • New York, New York, 미국, 10032
        • Site Reference ID/Investigator# 2614
      • New York, New York, 미국, 10065
        • Site Reference ID/Investigator# 5383
      • Rochester, New York, 미국, 14642
        • Site Reference ID/Investigator# 12306
      • Edmonton, 캐나다, T6G 1Z2
        • Site Reference ID/Investigator# 8941

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Diagnoses:

    • 1a/1b - lymphoid malignancy;
    • 2a, Arm A - follicular lymphoma;
    • 2a, Arm B - mantle cell, peripheral or cutaneous T-cell lymphomas including mycosis fungoides and Sezary syndrome or other indolent B-cell lymphomas such as marginal zone lymphoma;
  • Received at least 1 prior chemotherapy treatment regimen (P1a/1b) and relapsed or refractory disease (P2a).
  • Eastern Cooperative Oncology Group (ECOG) score of <= 1.
  • Magnetic Resonance Imaging (MRI)/computed tomography (CT) negative for subdural or epidural hematoma w/in 28 days prior to first dose, if clinically indicated.
  • Stable dose of Selective serotonin reuptake inhibitors (SSRI) antidepressants for at least 21 days prior to 1st dose.
  • Adequate bone marrow (BM) independent of any growth factor support (except with heavily infiltrated bone marrow (80% or more)):

    • Absolute Neutrophil Count (ANC) >= 1000/µL;
    • Platelets >= 100,000/mm3 (entry count must be independent of transfusion with in 14 days of Screening);
    • Hemoglobin >= 9.0/dL.
  • Adequate coagulation, renal, and hepatic function:

    • Serum creatinine <= 2.0 mg/dL or calculated creatinine clearance >= 50 mL/min;
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <= 3.0 x Upper Limit of Normal (ULN);
    • Bilirubin <= 1.5 x ULN;
    • Gilbert's Syndrome may have a bilirubin > 1.5 x ULN;
    • Coagulation: Activated partial thromboplastin time (aPTT), Prothrombin Time (PT), not to exceed 1.2 x ULN
  • Females must be surgically sterile, postmenopausal (at least 1 year), or negative results for a pregnancy test performed at Screening on a serum sample obtained with in 14 days prior to initial dose, and prior to dosing on a urine sample obtained on C1 D-3 (P1a) or Lead-in D1 (P1b, P2a) if > 7 days since serum results.
  • Females not surgically sterile or postmenopausal (at least 1 year) and non-vasectomized males must practice birth control.
  • P2a only: History of autologous stem cell transplant must be > 6 months post transplant with adequate BM independent of growth factor support per lab reference range at Screening as follows:

    • Absolute Neutrophil Count (ANC) >= 1,500/µL;
    • Platelets >= 125,000/mm3 (entry platelet count must be independent of transfusion with in 14 days of Screening);
    • Hemoglobin >= 10.0g/dL;
  • Measurable disease by International Working Group (IWG)/National Cancer Institute- sponsored Working Group (NCI-WG) criteria.
  • At least one of following for Pharmacodynamics (P2a):

    • archived diagnostic Formalin Fixed Paraffin Embedded (FFPE) tumor tissue with no intervening treatment since biopsy,
    • core needle biopsy of malignant lymph node, or
    • bone marrow aspirate or core positive for lymphoma.

Extension Study Inclusion Criteria Phase 2a subjects who enter the Extension Study must continue to meet all Inclusion and Exclusion criteria, with the exception of Inclusion Criterion regarding measurable disease by International Working Group (IWG)/National Cancer Institute- sponsored Working Group (NCI-WG) criteria and Inclusion Criteria regarding laboratory parameters for hematology, coagulation, and chemistry. Subjects entering the Extension Study must also have stable lab values per applicable laboratory reference ranges. In addition, subjects must also meet the following criteria:

  • Subjects must meet the following hematology and coagulation lab criteria:

    • Platelet counts must be >= 25,000/mm3 (untransfused). Platelet counts <= 50,000/mm3 must be stable and monitored at an increased frequency at the discretion of the investigator.
    • Absolute Neutrophil count (ANC) >= 500/µL. ANC >= 500/µL and < 1,000/µL should be monitored at an increased frequency at the discretion of the investigator.
    • Hemoglobin of >= 8.0 g/dL.
    • aPTT, PT is not to exceed 1.2 x ULN.
  • Chemistry values must not exceed Grade 2. Grade 2 chemistry labs should be monitored at an increased frequency at the discretion of the investigator. Subjects must meet the following chemistry criteria:

    • Serum creatinine <= 3.0 x the upper normal limit (ULN) of institution's normal range. * AST and ALT <= 5.0 x the upper normal limit (ULN) of institution's normal range.
    • Bilirubin <= 3.0 x ULN. Subjects with Gilbert's Syndrome may be allowed to have a Bilirubin > 3.0 x ULN based on a joint decision between the investigator and Abbott medical monitor.

Exclusion Criteria:

  • History of, or is, clinically suspicious for cancer-related Central Nervous System (CNS) disease, lymphoid or non-lymphoid.
  • Undergone an allogeneic or autologous stem cell transplant.
  • Underlying, predisposing condition of bleeding or currently exhibits signs of clinically significant bleeding.
  • Recent history of non-chemotherapy induced thrombocytopenic associated bleeding with in 1 year prior to first dose.
  • Active peptic ulcer disease or other hemorrhagic esophagitis/gastritis.
  • Active immune thrombocytopenic purpura or history of being refractory to platelet transfusions with in 1 year prior to first dose.
  • Significant history of cardiovascular disease, renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic, or hepatic disease.
  • Females pregnant or breast-feeding.
  • Positive for human immunodeficiency virus (HIV)
  • History of other active malignancies with in the past 3 years (P1a/1b) or past 5 years (P2a), except adequately treated in situ carcinoma of the cervix uteri; basal or squamous cell carcinoma; in situ carcinoma of the bladder; previous malignancy confined and surgically resected with curative intent.
  • Evidence of other clinically significant uncontrolled condition(s), including, but not limited to active systemic fungal infection; diagnosis of fever and neutropenia with in 1 week prior to study drug.
  • Received steroid therapy with in 7 days prior to 1st dose of study drug for anti-neoplastic intent.
  • Received any anti-cancer therapy, including chemotherapy, immunotherapy, radiotherapy, hormonal or any investigational therapy, with in 14 days prior to first dose of study drug, or has not recovered to <Gr2 clinically significant AE(s) /toxicity(s) of the previous therapy.
  • Received a biologic with in 30 days prior to first dose.
  • Currently receiving or requires anticoagulation therapy or any drugs or herbal supplements that affect platelet function, with the exception of low-dose anticoagulation medications that are used to maintain the patency of a central venous catheter.
  • Received aspirin with in 7 days prior to first dose and during ABT-263 administration.
  • Consumed grapefruit or grapefruit products with in 3 days prior to first dose.
  • P1a/1b only: Diagnosed with Posttransplant lymphoproliferative disorder (PTLD); Burkitt's, Burkitt-like, or HIV-associate lymphoma; lymphoblastic lymphoma/leukemia; or multiple myeloma.
  • Subject has received CYP3A inhibitors (e.g., ketoconazole, clarithromycin) within 7 days prior to the administration of the first dose of ABT-263 (P2a).
  • Subject had a prior significant toxicity from another Bcl-2 family protein inhibitor (P2a).

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Phase 1a and 1b
Relapsed or refractory lymphoid malignancies

Oral solution

Phase 1 dosing was under two different schedules: 14 days on drug, 7 days off or 21 days continuous dosing.

Oral solution and tablets

Phase 2a dosing under 21 day continuous dosing.

- 150 mg lead-in dose for 7-14 days followed by a 325 mg continuous once daily dose.

실험적: Arm A (Phase 2a)
Relapsed or refractory follicular lymphoma

Oral solution

Phase 1 dosing was under two different schedules: 14 days on drug, 7 days off or 21 days continuous dosing.

Oral solution and tablets

Phase 2a dosing under 21 day continuous dosing.

- 150 mg lead-in dose for 7-14 days followed by a 325 mg continuous once daily dose.

실험적: Arm B (Phase 2a)
Relapsed or refractory mantle cell, peripheral T-cell, cutaneous T-cell lymphoma including mycosis fungoides and Sezary syndrome, or other indolent B-cell lymphomas such as marginal zone lymphoma

Oral solution

Phase 1 dosing was under two different schedules: 14 days on drug, 7 days off or 21 days continuous dosing.

Oral solution and tablets

Phase 2a dosing under 21 day continuous dosing.

- 150 mg lead-in dose for 7-14 days followed by a 325 mg continuous once daily dose.

실험적: Extension Study
Relapsed or refractory follicular lymphoma or Relapsed or refractory mantle cell, peripheral T-cell, cutaneous T-cell lymphoma including mycosis fungoides and Sezary syndrome, or other indolent B-cell lymphomas such as marginal zone lymphoma

Oral solution

Phase 1 dosing was under two different schedules: 14 days on drug, 7 days off or 21 days continuous dosing.

Oral solution and tablets

Phase 2a dosing under 21 day continuous dosing.

- 150 mg lead-in dose for 7-14 days followed by a 325 mg continuous once daily dose.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Phase 1a: Determine dose limiting toxicity (DLT), maximum tolerated dose (MTD) and recommended Phase 2 dose (RPTD) and schedule - intermittent dosing.
기간: Repeating sequence of 14 days on therapy and 7 days off.
1a: Determination of dose limiting toxicity (DLT) and maximum tolerated dose (MTD) under a 14/21 day dosing schedule
Repeating sequence of 14 days on therapy and 7 days off.
Phase 1b: Determine dose limiting toxicity (DLT), maximum tolerated dose (MTD) and recommended Phase 2 dose (RPTD) and schedule - continuous dosing.
기간: 21 day continuous dosing.
Phase 1b: Determination of ABT-263 dose limiting toxicity (DLT) and maximum tolerated dose (MTD) under a 21 day continuous dosing schedule.
21 day continuous dosing.
Phase 2a: Continued assessment of safety profile at the recommended Phase 2 dose (RPTD) and schedule - continuous dosing.
기간: 21 day continuous dosing.
Phase 2a: Continued assessment of the safety profile of ABT-263 at the Recommended Phase 2 Dose (RPTD) and schedule under a 21 day continuous dosing.
21 day continuous dosing.
Phase 2a: Assessment of preliminary efficacy signals including biomarker assessment - continuous dosing.
기간: 21 day continuous dosing.
Phase 2a: Assessment of the preliminary efficacy signals of ABT-263, including biomarker assessment, at the Recommended Phase 2 Dose (RPTD) and schedule under a 21 day continuous dosing.
21 day continuous dosing.
Extension Study: Continued assessment of the safety profile of ABT-263
기간: 21 day continuous dosing
Continued assessment of the safety profile of ABT-263.
21 day continuous dosing
Extension Study: Continued assessment of the preliminary efficacy signals of ABT-263.
기간: day continuous dosing
Continued assessment of the preliminary efficacy signals of ABT-263.
day continuous dosing

2차 결과 측정

결과 측정
측정값 설명
기간
Phase 1a or Phase 1b safety assessment
기간: Repeating sequence of 14 days on therapy and 7 days off OR 21 day continuous dosing.
Assessment of the safety of ABT-263
Repeating sequence of 14 days on therapy and 7 days off OR 21 day continuous dosing.
Phase 1a, Phase 1b, or Phase 2a pharmacokinetic profile evaluation
기간: Repeating sequence of 14 days on therapy and 7 days off OR 21 day continuous dosing.
Evaluation of pharmacokinetic profile of ABT-263.
Repeating sequence of 14 days on therapy and 7 days off OR 21 day continuous dosing.
Phase 1a effect of food on bioavailability
기간: Repeating sequence of 14 days on therapy and 7 days off.
Evaluation of the effect of food on bioavailability
Repeating sequence of 14 days on therapy and 7 days off.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Mack Mabry, MD, AbbVie

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2006년 11월 1일

기본 완료 (실제)

2016년 10월 1일

연구 완료 (실제)

2016년 10월 1일

연구 등록 날짜

최초 제출

2006년 11월 30일

QC 기준을 충족하는 최초 제출

2006년 11월 30일

처음 게시됨 (추정)

2006년 12월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 8월 2일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 7월 28일

마지막으로 확인됨

2021년 7월 1일

추가 정보

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. .

구독하다