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临床试验/EUCTR2012-002208-41-ES
EUCTR2012-002208-41-ES进行中(未招募)1 期

An open-label phase II study of BKM120 in patients with relapsed and refractory diffuse large B-cell lymphoma, mantle cell lymphoma and follicular lymphoma

ovartis Farmacéutica S.A.0 个研究点目标入组 66 人开始时间: 2013年1月25日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
66

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

性别
All

入选标准

  • 1.Patient has a histologically confirmed diagnosis of mantle cell
  • lymphoma, follicular lymphoma, or diffuse large B cell lymphoma. 2.
  • Patient has relapsed or refractory disease and received at least one prior
  • therapy. 3. Patient with diffuse large B cell lymphoma has received or is
  • ineligible for autologous or allogeneic stem cell transplant. 4. Patient has
  • at least one measurable nodal lesion (?2 cm) according to Cheson
  • criteria (Cheson 2007). In case where the patient has no measurable
  • nodal lesions ? 2 cm in the long axis at baseline, then the patient must
  • have at least one measurable extra-nodal lesion. 5. Patient has an
  • Eastern Cooperative Oncology Group (ECOG) performance status ? 2. 6.
  • Patient has adequate bone marrow and organ function.
  • 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 33
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 33

排除标准

  • 1.1. Patient has received previous treatment with PI3K. 2. Patient has
  • evidence of graft versus host disease (GVHD). 3. Patient has active or
  • history of central nervous system (CNS) disease. 4. Patient has a
  • concurrent malignancy or has a malignancy within 3 years of study
  • enrollment (with the exception of adequately treated basal or squamous
  • cell carcinoma or non-melanomatous skin cancer). 5. Patient has a score
  • ? 12 on the PHQ-9 questionnaire. 6. Patient has a GAD-7 mood scale
  • score ? 15. 7. Pregnant or nursing women and who does not use highly
  • effective contraception methods to avoid becoming pregnant or
  • conciving offspring. Other protocol-defined inclusion/exclusion criteria

研究者

发起方
ovartis Farmacéutica S.A.

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