ISRCTN97388141已完成1 期
A Cancer Research UK Phase I trial of AT9283 (a selective inhibitor of aurora kinases) given over 72 hours every 21 days via intravenous infusion in children and adolescents aged 6 months to 18 years with relapsed and refractory acute leukaemia
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 7
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Morhologically proven acute lymphoblastic or acute myeloid leukaemia
- •2. Life expectancy of at least 8 weeks
- •3. Karnofsky / Lansky scale score of > or = to 50%
- •4. Biochemical indices within ranges as specified in the protocol
- •5. Aged > 6 months to <19 years
- •6. Written informed consent
排除标准
- •1. Chronic myeloid leukaemia
- •2. Cytotoxics, vincristine, anti-neoplastics within two weeks. One week for investigational medicinal products (except antibodies, for which a four week window must be observed), one week for protein kinase inhibitors and Intrathecal therapy before treatment
- •3. Central nervous system (CNS) disease
- •4. Ongoing toxic manifestations of previous treatments
- •5. Prior exposure to an aurora kinase inhibitor
- •6. Pregnant or lactating women
- •7. Fractional shortening of =29% on Echocardiogram
- •8. Previous anthracycline treatment with a cumulative dose equal to or greater than 450mg/m2 doxorubicin equivalent
- •9. Uncontrolled arterial hypertension defined as a systolic and / or diastolic blood pressure greater than or equal to the 95th percentile for age and height
- •10. Congenital heart disease, with the exception of patent foramen ovale or small muscular ventricular septal deficit (within the first year of life)
- •11. Active graft vs. host disease
- •12. Patients experiencing significant toxicity following Haematopoietic Stem Cell Transplant.
研究者
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