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临床试验/NL-OMON47367
NL-OMON47367已完成2 期

A Phase IIb, Open Label Study for the Detection of Dysplastic Colorectal Polyps during Colonoscopy after EMI-137 Injection in Patients with High Suspicion of Colorectal Cancer. - EMI-137 for detection of dysplastic colorectal polyps

Edinburgh Molecular Imaging Ltd.0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
200

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

年龄范围
18 至 64(—)

入选标准

  • 1. Signed informed consent prior to any study-mandated procedure;
  • 2. Healthy male or female subjects aged 18 years or older;
  • 3. Female subjects need to be either surgically sterile (has had a documented bilateral
  • oophorectomy and/or documented hysterectomy), post-menopausal (cessation of
  • menses for more than 1 year), or pre-menopausal with a negative urine pregnancy test
  • performed at screening and a negative urine pregnancy test performed within 24 hours
  • of administration of EMI-137 Injection. Pre-menopausal female subjects should also
  • employ an effective method of birth control up to 90 days after EMI-137 administration. Barrier contraceptives must be used throughout the study in both sexes.
  • 4. The subject has a positive FOB test or clinical suspicion on colorectal cancer and is scheduled to undergo a colonoscopy.
  • 5. The subject has a normal or clinically acceptable medical history, physical examination,
  • and vital signs findings at screening (within 35 days prior to administration of study
  • 6. The subject*s screening ECG and clinical laboratory tests are within normal limits, or if
  • any are outside of normal limits they are considered to be clinically insignificant.

排除标准

  • 1. If female, the subject is lactating or pregnant.
  • 2. The subject is being treated or has been treated with chemotherapy or radiation within
  • the 3 months before enrolment.
  • 3. A biopsy has been obtained from the colon within the 3 weeks before enrolment.
  • 4. The subject has been previously included in this study or another fluorescence IMP.
  • 5. Treatment with another IMP within 3 months prior to screening or more than 4 times in
  • the past year.
  • 6. Loss of blood outside the limits of Sanquin within 3 months prior to screening.
  • 7. The subject has had any significant change in their regular prescription or non-prescription medication between 14 days and 1 day prior to EMI-137 administration.
  • 8. The subject has a history of alcohol and/or drug abuse within the previous 12 months.

研究者

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