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
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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