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

28 de julho de 2021 atualizado por: 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).

Visão geral do estudo

Descrição detalhada

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

Tipo de estudo

Intervencional

Inscrição (Real)

81

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 99 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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).

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição sequencial
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.

Experimental: 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.

Experimental: 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.

Experimental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Phase 1a: Determine dose limiting toxicity (DLT), maximum tolerated dose (MTD) and recommended Phase 2 dose (RPTD) and schedule - intermittent dosing.
Prazo: 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.
Prazo: 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.
Prazo: 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.
Prazo: 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
Prazo: 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.
Prazo: day continuous dosing
Continued assessment of the preliminary efficacy signals of ABT-263.
day continuous dosing

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Phase 1a or Phase 1b safety assessment
Prazo: 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
Prazo: 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
Prazo: 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.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Diretor de estudo: Mack Mabry, MD, AbbVie

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo

1 de novembro de 2006

Conclusão Primária (Real)

1 de outubro de 2016

Conclusão do estudo (Real)

1 de outubro de 2016

Datas de inscrição no estudo

Enviado pela primeira vez

30 de novembro de 2006

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de novembro de 2006

Primeira postagem (Estimativa)

4 de dezembro de 2006

Atualizações de registro de estudo

Última Atualização Postada (Real)

2 de agosto de 2021

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de julho de 2021

Última verificação

1 de julho de 2021

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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