研究项目库 / NCT05006716

Tacabrutideg用于B-cell Malignancy的I 期 / II 期研究

这是一项关于B-cell Malignancy的I 期 / II 期研究,登记的药物或干预包括Tacabrutideg,当前状态为招募中。登记地点显示中国北京、广州、郑州、宜昌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B-cell Malignancy的I 期 / II 期研究,登记的药物或干预包括Tacabrutideg,当前状态为招募中。登记地点显示中国北京、广州、郑州、宜昌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

Tacabrutideg · I 期 / 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。

  • Peking Union Medical College Hospital · 北京
  • Nanfang Hospital, Southern Medical University · 广州
  • Henan Cancer Hospital · 郑州
  • Yichang Central Peoples Hospitaljiangnan Branch · 宜昌
  • Rui Jin Hospital Shanghai Jiao Tong University School of Medicine · 上海
  • Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciencestuanbo Branch · 天津
  • The First Affiliated Hospital of Wenzhou Medical University · 温州

公开的入选条件

  • 1. Confirmed diagnosis (per World Health Organization (WHO) guidelines, unless otherwise noted) of one of the following: Marginal Zone Lymphoma (MZL), R/R follicular lymphoma (FL), mantle cell lymphoma (MCL), chronic lymphocytic leukemia and small lymphocytic
  • 2. Participants who have previously received a covalently-binding Bruton´s tyrosine kinase (BTK) inhibitor (BTKi) in any line of therapy must have received treatment with the BTK inhibitor for ≥ 8 weeks (unless reason for discontinuation is intolerance).
  • 3. For dose-finding and dose-expansion, participants who had previously received a covalently-binding BTK inhibitor as monotherapy or in combination with other anticancer agents are eligible for the study if they meet any of the following criteria: discontinue
  • 4. Phase 2 Cohorts in R/R CLL/SLL, R/R MCL, and R/R WM only: Participants who previously received a BTKi are eligible if they had disease progression on only one regimen containing a covalent BTKi. Note: Participants may have received treatment with ≥ 2 differ
  • 5. Measurable disease by radiographic assessment or serum IgM level (WM only)
  • 6. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2
  • 7. Participants enrolling in the dose finding phase of the study may be previously treated with a BTKi or may be naïve to BTKi therapy depending on the diagnosis and country of enrollment; participants with MCL enrolling in the expansion cohorts (Phase 2) must

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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:NCT05006716;登记信息更新于 2026-09-11。

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