Breast Cancer Trial, Recruiting NCT06185569 Sponsor: Centre Hospitalier Universitaire de Besancon Condition: Breast Cancer
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Breast Cancer Trial, Recruiting

NCT06185569
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 who are 18 years of age or older
  • People who have been diagnosed with invasive breast cancer, confirmed through a biopsy or surgical sample
  • People whose breast cancer can be treated with surgery
  • People whose breast cancer is hormone receptor-positive (at least estrogen receptor-positive) and HER2-negative
  • People who have already had an Oncotype DX (ODX) test performed on their tumour (a genetic test used to guide treatment decisions)

Who may not be able to join:

  • People whose tumour cannot be surgically removed, or who are considered too unwell to safely undergo surgery
  • People who have two breast cancers at the same time with different biological characteristics (for example, one hormone receptor-positive/HER2-negative tumour alongside a triple-negative or HER2-positive tumour)
  • People who are currently receiving chemotherapy or hormone therapy before surgery (neoadjuvant therapy)
  • People whose cancer has spread to more than 4 lymph nodes
  • People whose breast cancer has already spread to other parts of the body at the time of diagnosis
  • People who have been diagnosed with another cancer in the past 10 years (skin cancers other than melanoma are generally excepted — confirm with trial site)
  • People who previously participated in the RxPONDER study in France
  • People who have formally declined to participate in the study by submitting a refusal letter to the investigator
  • People who do not have the legal capacity to consent to participation in a study

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 26 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: Elsa CURTIT, Centre Hospitalier Universitaire de Besancon

Phone: +33381219086

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
Centre Hospitalier Universitaire de Besancon
Registry
ClinicalTrials.gov
Start date
15 October 2023
Est. completion
1 September 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

to evaluate the clinical outcomes represented by iDFS in French early breast cancer patients with Oncotype DX (ODX) Breast Recurrence Score® (RS) results-guided therapy

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: 26 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