EUCTR2010-021444-18-GB进行中（未招募）1 期
TO ESTABLISH THE FEASIBILITY OF COMBINING EITHER THE TYROSINE KINASE INHIBITOR AC220 OR THE CXCR4 INHIBITOR PLERIXAFOR OR THE HSP90 INHIBITOR, GANETESPIB, WITH CHEMOTHERAPY IN OLDER PATIENTS WITH ACUTE MYELOID LEUKAEMIA AND HIGH RISK MYELODYSPLASTIC SYNDROME - AML 18 Pilot Trial
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 90
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
入选标准
- •1) They have one of the forms of AML, except Acute Promyelocytic Leukaemia as defined by the WHO Classifcation - this can be any type of de novo or secondary AML - or high risk MDS, defined as greater than 10% marrow blasts.
- •2) Serum creatinine = 1.5xULN.
- •3) White cell count of <30x10^9/L at diagnosis (for Plerixafor option only).
- •4) Serum potassium, magnesium and calcium levels should be at least within institutional normal limits.
- •5) Total serum bilirubin = 1.5xULN and serum aspartate transaminase and/or alanine transaminase = 2.5xULN
- •6) Sexually mature males must agree to use an adequate and medically accepted method of contraception throughout the study if their sexual partners are women of child bearing potential (WOCBP)
- •7) Over 60 years of age
- •8) Provided written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 80
排除标准
- •1)They have previously received cytotoxic chemotherapy for AML (hydroxycarbimide, or similar low-dose therapy, to control the white count prior to initiation of intensive therapy is not an exclusion)
- •2) They are in blast transformation of chronic myeloid leukaemia (CML)
- •3) They have a concurrent active malignancy excluding basal cell carcinoma
- •4) They are pregnant or lactating
- •5) They have Acute Promyelocytic Leukaemia
- •6) Known infection with human immunodeficiency virus (HIV)
- •7) Patients are not eligible for the AC220 option if they have:
- •-Uncontrolled or significant cardiovascular disease including:
- •-A myocardial infarction within 12 months
- •-Uncontrolled angina within 6 months
- •-Current, or history of, congestive heart failure New York Heart Association (NYHA) class 3 or 4, unless an echocardiogram or Multiple Gated Acquisition Scan performed either within 1 month prior to study screening or during screening results in a left ventricular ejection fraction that is =45% (or institutional lower limit of normal value)
- •-Diagnosed or suspected congenital long QT syndrome. Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or torsades de pointes); any history of arrhythmia will be discussed with the Sponsor's Medical Monitor prior to patient's entry into the study.
- •-Prolonged QTcF interval on pre-entry ECG (=450ms)
- •-Any history of second or third degree heart block (may be eligible if the patient currently has a pacemaker)
- •-Heart rate <50/min on pre-entry ECG
- •-Uncontrolled hypertension
- •-Obligate need for a cardiac pacemaker
- •-Complete left bundle branch block
- •-Atrial fibrillation
研究者
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