CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,514 enrolled
Drug / intervention
Circulating tumor DNA assaygenetic
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02808884
NCT02808884N/ACompleted

Cancer DNA Screening Pilot Study (CANDACE)

British Columbia Cancer Agency·interventional·Posted Jun 22, 2016·Updated Aug 24, 2020

In Brief

A clinical study evaluating Circulating tumor DNA assay for Circulating Tumor Cells. Completed, enrolled 1,514 participants across 1 site.

Detailed Summary

The investigators have developed an assay that can sensitively and specifically detect DNA mutations circulating in human plasma that may be indicators of the presence of a solid tumor. This study is a pilot study to measure positive and negative predictive values of this assay as an indicator of the presence of a tumor in normal subjects

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 22, 2016
Enrollment StartSep 19, 2016
Primary CompletionJun 10, 2019
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 10.0 years ago

Interventions

Circulating tumor DNA assaygenetic

Blood samples will be separated into plasma and cellular fraction including erythrocytes and buffy coat.The plasma fraction will be placed in a separate tube and frozen for subsequent analysis. Frozen plasma samples, de-identified, will be delivered to Pathway Genomics where DNA content will be analyzed with a circulating tumor DNA assay employing the UBC/Boreal Genomics enrichment technology. All of the participants' plasma will be sent to Pathway, where it will be used up in the assay. Circulating tumor DNA assay results (raw sequencing data) from Pathway Genomics will be returned to UBC and analyzed for the presence of cancer mutations. Any samples showing activating mutations above the assay's technical Limit of Detection (LOD) will be called positive. One exception will be made for TP53 mutations that are known to exist in some normal individuals at low levels. For these mutations, a level of 0.1% will be set, above which the sample will be called positive.