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临床试验/NCT07168876
NCT07168876招募中不适用

Clinical Validation Cross-sectional Study for Colorectal Cancer Assessment Using Delta-HLD Technology (CLIMBED)

Epiliquid Holding, Inc1 个研究点 分布在 1 个国家目标入组 3,200 人开始时间: 2024年4月4日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
3,200
试验地点
1
主要终点
Sensitivity of colorectal cancer detection

研究概览

简要总结

CLIMBED (Colon cancer Liquid biopsy Investigation of Methylation-based Biomarkers Evaluation using Delta-HLD) is a non-randomized, observational, cross-sectional clinical validation study designed to assess the performance of Delta-HLD, Epiliquid's proprietary liquid biopsy technology, for colorectal cancer (CRC) detection. The study will evaluate the test performance in an average-risk population for CRC undergoing screening colonoscopy, which will serve as the gold standard reference.

详细描述

Colorectal cancer (CRC) is one of the most common cancers worldwide and among the leading causes of cancer-related mortality. Early detection substantially improves survival; however, adherence to existing screening strategies remains suboptimal across different regions. CLIMBED is a non-randomized, observational, cross-sectional clinical validation study designed to assess the performance of Epiliquid's Delta-HLD liquid biopsy technology, which detects methylation-based epigenetic biomarkers in plasma using PCR. The study will enroll 3200 participants between 45 and 75 years of age, representing an average-risk CRC population. All participants will undergo screening colonoscopy, which will serve as the gold standard for comparison. The primary endpoints are sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of the Delta-HLD technology for CRC detection in cfDNA. Secondary endpoints include the capacity of the test to identify precursor lesions. Statistical analysis will be based on ROC curves and AUC to determine diagnostic performance.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

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

  • Men and women aged 45-75 years
  • Indication of colorectal cancer screening colonoscopy by treating physician

排除标准

  • First-degree family history of CRC
  • Inflammatory bowel disease (ulcerative colitis, Crohn's disease)
  • Other malignancies within 5 years
  • Known hereditary CRC syndromes (Lynch, FAP)
  • Major trauma, surgery, transfusion in past 30 days
  • Current participation in an interventional clinical trial

结局指标

主要结局

Sensitivity of colorectal cancer detection

时间窗: 18 months

Sensitivity and specificity of the Delta-HLD test for detection of colorectal cancer

Specificity of advanced neoplasia detection

时间窗: 36 months

Specificity of colorectal cancer detection

次要结局

  • Accuracy of colorectal cancer precursor lesions detection(36 months)
  • Predictive values(36 months)

研究者

发起方
Epiliquid Holding, Inc
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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