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临床试验/EUCTR2013-003749-40-AT
EUCTR2013-003749-40-AT进行中(未招募)1 期

A Phase Ib/II, open label study evaluating the safety and pharmacokinetics of GDC-0199 (ABT-199) in combination with Rituximab (R) or Obinutuzumab (G) plus cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) in patients with B Cell non-hodgkin's lymphoma (NHL) and DLBC

F. Hoffmann- La Roche Ltd.0 个研究点目标入组 264 人开始时间: 2015年5月19日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
264

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • General Inclusion Criteria:
  • - Patients, age >= 18 years
  • - At least one bi-dimensionally measurable lymphoma lesion defined as
  • > 1.5 cm in its longest dimension which is also FDG avid by screening
  • - Ability and willingness to comply with the study protocol procedures
  • - Confirmed availability of archival or freshly biopsied tumor tissue prior
  • to study enrollment
  • - ECOG performance status of 0, 1, or 2
  • - Adequate hematologic function
  • - For female patients of childbearing potential and male patients with
  • female partners of childbearing potential, agreement to use highly
  • effective forms of contraception
  • Dose Finding Portion of the Study:
  • - Patients must have histologically confirmed B-cell non-Hodgin's
  • Lymphoma (NHL)
  • - Patients must have never received previous R-CHOP treatment
  • - Any relapsed/refractory patients that are enrolled during the dose
  • escalation should have received only a single previous treatment
  • Phase II Portion of the Study:
  • - Patients must have previously-untreated CD20-positive diffuse large,
  • B-cell lymphoma
  • - International prognostic index (IPI) score must be 2-5
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 125
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 125

排除标准

  • General Exclusion Criteria:
  • - Contraindication to receive any of the individual components of CHOP,
  • rituximab or obinutuzumab
  • - CNS lymphoma or primary mediastinal DLBCL
  • - Vaccination with live vaccines within 28 days prior to randomization
  • - History of other malignancy that could affect compliance with the
  • protocol or interpretation of results
  • - Evidence of significant, concomitant disease or illness
  • - Use of CYP3A inhibitors or inducers within 7 days of the first dose of
  • - Recent major surgery
  • - Women must not be pregnant or breastfeeding
  • Dose Finding Portion of the Study:
  • - Histologically confirmed mantle cell lymphoma (MCL) or small
  • lymphocytic lymphoma (SLL)
  • Phase II Portion of the Study:
  • - Patients with transformed lymphoma (patients with discordant bone
  • marrow involvement [i.e., low grade histology in bone marrow] may be
  • considered after discussion with the Medical Monitor)
  • - Prior therapy for non-hodgkin's lymphoma (NHL)

研究者

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