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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
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
Participation Requirements
Sex: Female
Minimum Age: 40
Maximum Age: 70
Healthy Volunteers: t
View:

• Group 1 - Breast Cancer:

• Age between 40 and 70 years Diagnosis of breast cancer at any stage No prior surgical treatment No prior antineoplastic treatment Pathology report available at the time of enrollment Signed informed consent

• Group 2 - No Cancer (Control):

• Age between 50 and 70 years No diagnosis or personal history of any type of cancer Digital mammography and breast ultrasound showing no breast pathology (BI-RADS 1 or 2) Signed informed consent

Locations
Other Locations
Argentina
DIM Centros de Salud
RECRUITING
Buenos Aires
Contact Information
Primary
Adriana De Siervi, PhD in Molecular Biology
adesiervi@oncoliq.bio
+54 11 3269 5832
Backup
Camila Zaslavsky, Pharmacist
camila@oncoliq.bio
+54 11 2164 1626
Time Frame
Start Date: 2025-10-17
Estimated Completion Date: 2026-02-28
Participants
Target number of participants: 300
Treatments
Breast Cancer Cohort
Participants with a confirmed diagnosis of breast cancer, prior to surgery or systemic treatment.
Healthy Control Cohort
Cancer-free volunteers confirmed by breast imaging (BI-RADS 1 or 2) and without a prior history of cancer.
Related Therapeutic Areas
Sponsors
Leads: Oncoliq US Inc

This content was sourced from clinicaltrials.gov