RecruitingNCT07331506

Validation of the Oncoliq Test for the Early Detection of Breast Cancer.


Sponsor

Oncoliq US Inc

Enrollment

300 participants

Start Date

Oct 17, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

Cancer continues to be one of the most significant public health issues worldwide. Thanks to early detection, the mortality rate of certain types of cancer has decreased significantly. However, the lack of accessible, low-cost, non-invasive, non-toxic, and easy-to-implement diagnostic methods results in late diagnoses, leading to 1 in every 6 people dying from cancer today. MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression and are found both inside cells and in bodily fluids such as blood and urine. Several studies have demonstrated their role in human diseases, especially cancer, where tumors release miRNAs into the bloodstream that can be used as biomarkers for early detection. The research and development team at Oncoliq SAS identified a panel of miRNAs associated with breast cancer, with a detection performance of 82% sensitivity and 83% specificity, validated in exploratory and preliminary confirmatory studies. These results led to the filing of a patent based on liquid biopsy technology. The objective of this protocol is to establish a panel of miRNAs for the early detection of breast cancer using samples from breast cancer patients and a cancer-free control group. Validation of the miRNAs will be carried out through RT-qPCR. This stage constitutes the analytical validation of the biomarkers, with the goal of developing an algorithm capable of classifying individuals with and without breast cancer. In future stages, a pilot clinical trial is planned to evaluate test implementation and clinical validation.


Eligibility

Sex: FEMALEMin Age: 40 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is validating a new blood test called the Oncoliq test for the early detection of breast cancer. The test looks for cancer signals in the blood (liquid biopsy), and researchers want to confirm how accurately it can distinguish between women with breast cancer and healthy women. **You may be eligible if (Group 1 — with breast cancer)...** - You are between 40 and 70 years old - You have been diagnosed with breast cancer at any stage - You have not yet had surgery or started cancer treatment - A pathology report is available at enrollment **You may be eligible if (Group 2 — control group, no cancer)...** - You are between 50 and 70 years old - You have no personal history of any cancer - Your recent mammogram and breast ultrasound are normal (BI-RADS 1 or 2) **You may NOT be eligible if...** - You have refused to sign the informed consent form - You have communication difficulties (severe hearing loss, blindness, cognitive impairment, or dementia) - A blood draw is not feasible or poses a medical risk - You have a personal history of previous cancer Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERPeripheral blood draw

Collection of a blood sample for plasma isolation and miRNA analysis.


Locations(1)

DIM Centros de Salud

Buenos Aires, Buenos Aires, Argentina

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NCT07331506


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