研究项目库 / NCT02436707

Ibrutinib用于淋巴瘤的II 期研究

这是一项关于淋巴瘤的II 期研究,登记的药物或干预包括Ibrutinib;Rituximab;Gemcitabine;Dexamethasone;Cisplatin;Mesna;Cyclophosphamide;Etoposide;G-CSF;Selinexor,当前状态为研究进行中,已停止招募。登记地点显示中国Calgary、Edmonton、Vancouver、Winnipeg等城市有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

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这是一项关于淋巴瘤的II 期研究,登记的药物或干预包括Ibrutinib;Rituximab;Gemcitabine;Dexamethasone;Cisplatin;Mesna;Cyclophosphamide;Etoposide;G-CSF;Selinexor,当前状态为研究进行中,已停止招募。登记地点显示中国Calgary、Edmonton、Vancouver、Winnipeg等城市有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

药物或干预

Ibrutinib;Rituximab;Gemcitabine;Dexamethasone;Cisplatin;Mesna;Cyclophosphamide;Etoposide;G-CSF;Selinexor · II 期

中国哪些地方有记录

以下地点来自登记信息,不代表此刻仍有名额;请向研究中心确认最新情况。

  • Arthur J.E. Child Comprehensive Cancer Centre · Calgary
  • Cross Cancer Institute · Edmonton
  • BCCA - Vancouver · Vancouver
  • CancerCare Manitoba · Winnipeg
  • QEII Health Sciences Centre · Halifax
  • Kingston Health Sciences Centre · Kingston
  • Ottawa Hospital Research Institute · Ottawa
  • University Health Network · Toronto
  • CHUM-Centre Hospitalier de l'Universite de Montreal · Montreal
  • CHU de Quebec-Hopital l'Enfant-Jesus (HEJ) · Québec
  • Allan Blair Cancer Centre · Regina

公开的入选条件

  • * Patients with histologic diagnosis for one of the following histologies according to the World Health Organization: documented at initial diagnosis or at relapse:
  • Diffuse large cell lymphoma, B-cell (includes primary mediastinal B-cell lymphoma, T-cell rich B-cell lymphoma);
  • Previous indolent lymphoma (follicular lymphoma, marginal zone lymphoma, including extranodal MALT lymphoma, lymphoplasmacytoid lymphoma) with transformation to diffuse large B-cell lymphoma at most recent relapse (biopsy proof of transformation is mandatory);
  • Unclassifiable B-cell lymphoma with indeterminate features between diffuse large B-cell lymphoma and Burkitt lymphoma.
  • * Biopsy proof of disease at initial diagnosis is mandatory. A repeat biopsy in primary refractory disease is preferred but not mandatory to confirm progressive disease. A biopsy at relapse is preferred but not mandatory. Participating centres must designate a
  • * Patients must be CD20+ in order to be eligible for the study.
  • * Clinically and/or radiologically measurable disease (one site bidimensionally measurable). Measurements/ evaluations must be done within 28 days prior to randomization.
  • * Prior FDG-PET scan, if done at baseline, must be positive (known FDG-avid lymphoma)

联系前需要确认

请继续确认中心是否启动、疾病分型、既往治疗、检查费用和知情同意安排。

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登记号:NCT02436707;登记信息更新于 2026-09-17。

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