Breast Cancer Trial, Recruiting NCT04874064 Sponsor: Jewish General Hospital Condition: Breast Cancer
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Breast Cancer Trial, Recruiting

NCT04874064
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People diagnosed with triple negative breast cancer (a type of breast cancer that tests negative for certain proteins: ER, PR, and HER2, or where ER is found in less than 10% of cells).
  • People who have completed at least 8 weeks of chemotherapy given before surgery (called neoadjuvant chemotherapy).
  • People who are waiting for surgery and whose scans or physical examination show signs that some cancer may still be present, as determined by their treating doctor.
  • People who have already had surgery and whose tissue sample examined in a lab confirmed that some cancer remained after surgery.
  • People who are able to attend clinic appointments within 6 weeks after surgery and for the following 6 months.
  • People who are willing to provide a series of blood samples during the study.
  • People who are able to follow the study schedule, including appointments, tests, and other study requirements.

Who may not be able to join:

  • People whose cancer has spread to other parts of the body (metastatic disease), based on physical examination or scans.
  • People whose breast cancer has come back after a previous diagnosis (a recurrence).
  • People who have not had chemotherapy before surgery, or who had less than 8 weeks of it.
  • People who received radiation treatment before their surgery.
  • People who are not able to sign or understand the consent form for the study.
  • People with a known HIV or hepatitis infection.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Mark Basik, Dr, Study Principal Investigator

Phone: 514-340-8222

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Jewish General Hospital
Registry
ClinicalTrials.gov
Start date
5 December 2019
Est. completion
1 December 2027

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Develop signatures of good and poor outcome as well of tumor response to chemotherapy in TNBCs by integrating multidimensional profiling of both tumor and liquid biopsies making use of Artificial Intelligence (AI) tools

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov