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临床试验/NCT02393027
NCT02393027终止早期 1 期

Quantification of Dopamine Active Transporter (DAT) in Humans: Validation of a New Radiophamaceutical, the [18F] LBT-999

University Hospital, Tours1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2015年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
终止
入组人数
16
试验地点
1
主要终点
Binding potential of [18F] LBT-999

研究概览

简要总结

Idiopathic Parkinson's disease (IPD) is a degenerative disease affecting the dopaminergic system. Clinical symptoms of IPD commonly begin after the loss of at least 40 to 50% of striatal dopaminergic terminals (specially putaminal terminals).

The Dopamine neuronal transporter (DAT) is a highly expressed protein in the membrane of presynaptic nigrostriatal dopaminergic terminals. The use of a DAT's radioligand in the initial stages of the disease would lead to an early detection of nigral cell loss.

Currently, only one DAT's radioligand has obtained marketing authorization in France, the 123I-FPCIT, for use in Single Photon Emission Computed Tomography (SPECT).

Otherwise, the Positron Emission Tomography (PET), a more sensitive technology than SPECT with higher resolution has become for a few years the new gold standard for visual analysis and quantification of neurotransmission systems (including the dopaminergic system).

A DAT tracer labelled with Carbon 11 ([11C] PE2l) have been developed and is currently used as a reference in various research centers.

However, in order to enable a clinical use of this tracer (which currently can't be because of the too short period of Carbon 11), the unit INSERM U930 "Imaging and Brain" in collaboration with the CERRP (Center for Studies and Research on Radiopharmaceuticals) developed a new version of this tracer, labelled with 18-fluor: the [18F] LBT-999.

The main goal of this study is to compare the [18F] LBT-999 uptake between a group of patients suffering from a Parkinsonien syndrome to a group healthy volunteers.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Criteria common to all participants:
  • Age between 45 and 75 years old
  • Signed informed consent
  • Affiliated to a social security system
  • Criteria for patients:
  • idiopathic Parkinson's disease according to the UKPDSBB criteria
  • stage 1-3 Hoen and Yahr (unilateral disease to moderate or mild bilateral disease in a self patient )
  • Criteria for healthy volunteers:
  • matching according to age (± 5 years)

排除标准

  • Criteria common to all participants:
  • history of taking an antipsychotic or any other drug with a dopaminergic effect in the previous 6 months
  • contraindications to MRI
  • person with severe claustrophobia
  • patient with a legal protection measure
  • alcohol or drug abuse history (in the past 10 years)
  • history of progressive disease that can affect the central nervous system (blood pressure greater than or equal to 180/100 mmHg, chronic lung disease with hypoxia, heart failure stage 4)
  • all medical and surgical affection older than 3 months
  • history of stroke
  • history of head trauma (coma> 24h)
  • pregnancy or lactating woman without reliable contraception

研究组 & 干预措施

patients

Experimental

10 idopathic parkinson disease

干预措施: [18F] LBT-999 PET (Drug)

controls subjects

Active Comparator

10 healthy controls (no parkinson disease)

干预措施: [18F] LBT-999 PET (Drug)

结局指标

主要结局

Binding potential of [18F] LBT-999

时间窗: one year

次要结局

  • DAT striatal density by estimating the LBT-999 distribution volume(one year)
  • presence of lipophilic metabolites(one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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