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Study identifier: NCT06268405 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Positron Emission Mammography and Liquid Biopsy in Women With High-risk Breast Screenings

Condition: Breast Cancer  ·  Sponsor: University Health Network, Toronto

PhaseNA
Planned participants100
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this research study is to evaluate the performance of two experimental tests, namely Liquid Biopsy and Positron Emission Mammography (PEM) in women at high risk of breast cancer. The plan for this study is to assess whether findings from the combination or each individual test can assist radiologists in visualizing and characterizing beast abnormalities. Liquid Biopsy is a blood test that can detect early tumours in patients with malignancies, while PEM is an imaging tool equipped with a high-resolution camera that uses a low dose of injected positron emitting isotope to locate breast tumours. Participation in this study entails a blood draw for Liquid Biopsy test and a PEM imaging exam before undergoing a magnetic resonance imaging (MRI) - guided biopsy for a suspicious breast lesion. If PEM and/or Liquid Biopsy provide accurate information to assist radiologists in visualizing and characterizing breast abnormalities, this method may serve as the first step towards establishing these genomic and new imaging technologies as new diagnostic modalities and ultimately reduce the unnecessary biopsies and anxiety in high-risk populations.

This description comes directly from the study's public registry record.

Talk to the study team

Samira Taeb, MSc  ·  416-946-4501  ·  samira.taeb2@uhn.ca

Vivianne Freitas, MD  ·  416-946-2000  ·  vivianne.freitas@uhn.ca

Always discuss trial participation with your own doctor first.

Locations (1)

University Health NetworkToronto, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06268405