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临床试验/EUCTR2017-002762-44-IE
EUCTR2017-002762-44-IE进行中(未招募)1 期

A phase I/II study evaluating the safety and activity of Pegylated recombinant human Arginase (BCT-100) in Relapsed/refractory cancers of Children and young adults - PARC

niversity of Birmingham0 个研究点目标入组 64 人开始时间: 2019年6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)
入组人数
64

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

  • Aged 2- <25 years old
  • Histologically confirmed disease in one of the following four cohorts. Patients with and without metastatic lesions are eligible.
  • oCohort 1 - Acute lymphoblastic leukaemia (ALL) and acute myeloid leukaemia (AML)
  • oCohort 2 - Neuroblastoma
  • oCohort 3 - Sarcoma
  • oCohort 4 - High grade glioma (as defined by 2016 WHO CNS classification)
  • Radiological or laboratory evidence of disease progression (during or after completion of first line treatment) or any subsequent recurrence
  • Measurable bone marrow disease (cohort 1) or at least one evaluable radiological site of disease (cohort 2, 3 and 4)
  • Adequate liver function defined as a total bilirubin <1.5x the upper limit of normal for age and ALT <3x the upper limit of normal for age
  • Normal ECG
  • Documented negative pregnancy test for female patients of childbearing potential within 7 days of trial entry
  • Sexually active patients must agree to use adequate and appropriate contraception while on study drug and for 12 months following treatment discontinuation
  • Written informed consent given by patient and/or parents/legal representative
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 60
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 8
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Previous treatment with another therapeutic arginine depleting drug (bacterial or human) or arginase inhibitor
  • Presence of any = CTCAE grade 3 clinically significant treatment-related toxicity from prior therapies
  • Pregnant or lactating female
  • Evidence of uncontrolled infection
  • History of an anaphylactic (i.e. life-threatening) reaction to kanamycin.

研究者

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