OncoSweep Cancer Spotlight and Spectrum Product Line

Trial Title: OncoSweep Cancer Spotlight and Spectrum Product Line

NCT ID: NCT06261294

Condition: Lung Cancer

Conditions: Keywords:
cancer study

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Diagnostic Test
Intervention name: OncoSweep Lung Spotligh
Description: This study is to develop and validate the performance of OncoSweep Lung Spotlight for detecting circulating miRNA expression, ctDNA methylation status, platelet RNA, and tumor marker expressions by utilizing real-time polymerase chain reaction (qPCR). The method is to collect venous blood from subjects during their routine visit to the healthcare facilities.
Arm group label: two group Study arm determination based

Summary: CONQUER cancer study: To collect blood samples from cancer and non-cancer participants for development and validation of the 'OncoSweep Cancer Spotlight and Spectrum Product Line'

Detailed description: OncoSweep Cancer Spotlight and Spectrum Product Lines are qualitative in vitro diagnostic devices testing plasma specimens for detecting circulating miRNA expression, ctDNA methylation status, platelet RNA analysis, and tumor marker expressions by utilizing real-time polymerase chain reaction (qPCR) and next-generation sequencing (NGS). This is a two-arm, open-label, non-randomized controlled pilot study intends to screen adults 18 years or older, who are treatment-naïve for cancers and have pulmonary nodules or mass detected by low-dose computerized tomography (LDCT) or standard computerized tomography (CT) scans. OncoSweep Lung Spotlight will be utilized with venous blood samples collected in the healthcare facility where the study is being conducted. The X-ray, LDCT/ standard CT scan, blood laboratory test data, or biopsy results will be collected from the control group, and the blood sample will be analyzed by OncoSweep Lung Spotlight. Results generated from both groups will be evaluated against each other. The result of OncoSweep Lung Spotlight provides additional evidence to support or assist medical diagnoses when used in combination with LDCT/ standard CT scan data.

Criteria for eligibility:

Study pop:
This is a two-arm, open-label, non-randomized controlled pilot study intended to screen adults of 18 years or older, who are treatment-naïve for cancers, or who have pulmonary nodules or masses detected by LDCT or standard CT scan, utilizing OncoSweep Lung Spotlight with venous blood sample collected in the healthcare facility where the study is being conducted.

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Inclusion 1. Individual who is not mentally impaired, capable to read, understand, and is willing to provide signed and dated informed consent form. 2. Individual is aged 18 years old or above. 3. Individual who is willing to provide information on the given questionnaire. Test group: Individual was diagnosed with pulmonary nodules or masses by low-dose CT (LDCT)/ CT, and evaluated by the physician needed to conduct a biopsy or/ and surgery has been arranged. Control group: Individual is willing to undergo LDCT or CT scan with 3-5 mm spatial z-axis resolution, pulmonary function examination, X-ray, laboratory blood test, and blood drawing. 4. Control group: Individual has no abnormal finding from LDCT or CT scan with 3-5 mm spatial z-axis resolution and pulmonary function examination(FEV1/FVC Ratio≧70%). 5. Individual did not donate blood or receive blood transfusion within two months before joining the study. Exclusion Criteria: - Exclusion 1. Individual who is not suitable for participating as per Investigator's judgement. 2. Individual who has undergone gene therapy or related product within one year prior to enrolling in this study. 3. Individual who is attending another clinical study at the time of enrollment. 4. Individual who is known to be pregnant. 5. Individual who has received a vaccine within two weeks. 6. Individual who has a history of any cancer occurrences other than lung cancer.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Mackay Memorial Hospital

Address:
City: Taipei
Zip: 104217
Country: Taiwan

Status: Recruiting

Contact:
Last name: Sheng-Hsiung Yang

Phone: +886 2 2543-3535
Email: lazatemax@gmail.com

Start date: May 23, 2023

Completion date: March 20, 2026

Lead sponsor:
Agency: Pharus Taiwan, Inc.
Agency class: Industry

Source: Pharus Taiwan, Inc.

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06261294