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临床试验/NCT03164486
NCT03164486进行中(未招募)早期 1 期

First-in-Human Positron Emission Tomography Study Using the 18F-αvβ6-Binding-Peptide

Julie L. Sutcliffe, Ph.D1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2016年11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
进行中(未招募)
发起方
入组人数
27
试验地点
1
主要终点
Assessment of safe administration of 18F-αvβ6-BP

研究概览

简要总结

This clinical trial studies the side effects of 18F-alphavbeta6-binding-peptide and how well it works in imaging patients with primary or cancer that has spread to the breast, colorectal, lung, or pancreatic. Radiotracers, such as 18F-alphavbeta6-binding-peptide, may improve the ability to locate cancer in the body.

详细描述

PRIMARY OBJECTIVES:

I. To determine the safety, biodistribution and dosimetric properties of 18F-alphavbeta6-binding peptide (BP) in normal tissues and malignancies in cancer patients and correlate concordance with alphavbeta6 expression.

OUTLINE:

Patients receive 18F-alphavbeta6-BP intravenously (IV) and then undergo positron emission tomography (PET) scans over 30 minutes each at 30, 60, 120, and 180 minutes post-injection.

After completion of study, patients are followed up for up to 6 months.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Diagnosed with primary or metastatic cancer in one or more of the following locations: breast, colorectal, lung, pancreas
  • Eastern Cooperative Oncology Group (ECOG) performance score of 0-1
  • Will sign the Institutional Review Board (IRB)-approved consent form
  • Able to remain motionless for up to 30-60 minutes per scan

排除标准

  • Creatinine > 2 x upper limit of normal
  • Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) > 2 x upper limit of normal
  • Life expectancy < 3 months (mo)
  • Women who are pregnant or breast-feeding
  • Patients who cannot undergo PET/compute tomography (CT) scanning
  • Lack of availability for follow-up assessments
  • Participation in another clinical trial involving an investigational agent within 4 weeks of enrollment

研究组 & 干预措施

18F-αvβ6-BP

Experimental

Patients receive 18F-alphavbeta6-BP IV and then undergo 4 PET scans over 30 minutes each at 30, 60, 120, and 180 minutes post-injection.

干预措施: 18F-αvβ6-BP (Drug)

结局指标

主要结局

Assessment of safe administration of 18F-αvβ6-BP

时间窗: Up to 6 months

Assessed by measures and/or changes in a given vital sign

次要结局

  • Measurement of 18F-αvβ6-BP accumulation in tumors(Up to 6 months)
  • Level of αvβ6-BP expression in tumors(Up to 6 months)

研究者

发起方
Julie L. Sutcliffe, Ph.D
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Julie L. Sutcliffe, Ph.D

Principal Investigator

University of California, Davis

研究点 (1)

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