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临床试验/EUCTR2015-001901-15-ES
EUCTR2015-001901-15-ES进行中(未招募)1 期

atural Killer cell infusion as consolidation therapy in children and adolescents with acute myelogenous leukemia.

Antonio Pérez Martínez0 个研究点开始时间: 2015年11月5日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

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. Patients aged between 0 and 21 years diagnosed with AML in first cytologic remission who have completed induction and consolidation chemotherapy phase, and do not comply criteria for allogeneic HSCT. That is, patients who have responded well to induction lacking HLA identical related donor and have high-risk cytogenetic abnormalities
  • 2. Lansky / Karnofsky index > 60%.
  • 3. Functional disorders of organs (liver, kidney, respiratory) mild-moderate (<4), according to the criteria of the National Cancer Institute (NCI CTCAE v4).
  • 4. Left Ventricule ejection fraction> 39% .
  • 5. Grant informed consent in accordance with current legislation .
  • 6. Presence of a haploidentical donor.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 35
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 35
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Patients with a history of poor compliance.
  • 2. Patients who after a psycho-social assessment are censored as unfit for the procedure:
  • psycho-social situation that makes it impossible proper participation in the study.
  • Patients with disease secondary to emotional or psychological problems such as PTSD, phobias, delusions, psychosis, with support request by specialists.
  • Evaluation of the involvement of the family in the patient's health.
  • Inability to understand information about the trial.
  • 3. Severe alteration of  functional organs (liver, kidney, respiratory) (4), according to the criteria of the National Cancer Institute (NCI CTCAE 4.3).
  • 4. Contraindications, interactions, precautions for use and dose reductions indicated in the corresponding summary of product characteristics should be considered.

研究者

发起方
Antonio Pérez Martínez

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