EUCTR2016-002205-19-IT进行中（未招募）1 期
A Phase 2, Multicenter, International, Open-Label, Safety and EfficacyStudy of INCB050465 in Subjects With Relapsed or Refractory DiffuseLarge B-Cell Lymphoma - CITADEL-202
INCYTE CORPORATIO0 个研究点目标入组 60 人开始时间: 2020年11月4日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
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
- •Men and women, aged 18 years or older.
- •Relapsed or refractory DLBCL, which has been histologically
- •documented, defined as having received at least 2 but no more than 5
- •prior treatment regimens (eg, an anti-CD20 antibody, an anti-CD20
- •antibody with or without chemotherapy, or chemotherapy alone) and
- •ineligible for high-dose chemotherapy supported by autologous stem cell
- •transplant.
- •Must have = 1 measurable (= 2 cm in longest dimension) or = 1
- •measurable extranodal lesion (> 1 cm in longest dimension) lesion on
- •computed tomography (CT) scan or magnetic resonance imaging (MRI).
- •Subjects must be willing to undergo an incisional or excisional lymph
- •node biopsy of accessible adenopathy or provide the most recent,
- •available archived tumor biopsy.
- •Eastern Cooperative Oncology Group performance status 0 to 2.
- •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 66
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 54
排除标准
- •Primary mediastinal (thymic) large B-cell lymphoma.
- •Known brain or central nervous system metastases or history of
- •uncontrolled seizures.
- •Allogeneic stem cell transplant within the last 6 months, or active graft
- •versus host disease following allogeneic transplant, or autologous stem
- •cell transplant within the last 3 months.
- •Use or expected use during the study of any prohibited medications,
- •including potent cytochrome P450 3A4 inhibitors or inducers within 14
- •days or 5 half-lives (whichever is longer) before the first dose of study
- •Prior treatment with the following:
- •- Group A: Prior treatment with a selective phosphatidylinositol 3-
- •kinase (PI3K) d inhibitor (eg, idelalisib), a pan-PI3K inhibitor, or a BTK
- •inhibitor (eg, ibrutinib).
- •- Group B: Prior treatment with a selective PI3Kd inhibitor (eg,
- •idelalisib) or a pan-PI3K inhibitor.
研究者
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