Phase 2 Breast Cancer Trial, Recruiting NCT07108309 Sponsor: Biocad Condition: Breast Cancer
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Phase 2 Breast Cancer Trial, Recruiting

NCT07108309
Recruiting Phase 2

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 have given signed consent to take part and are able to follow the study requirements.
  • People aged 18 or older but under 75 years old at the time of signing the consent form.
  • People who have a laboratory-confirmed diagnosis of triple-negative breast cancer (TNBC), based on specific test results showing low or absent levels of certain receptors (ER, PR, and HER2).
  • People whose TNBC has continued to grow or has come back during or after systemic (whole-body) treatment.
  • People who have received at least one round of systemic treatment for advanced or metastatic TNBC, or whose cancer came back or worsened either during or within 6 months of finishing post-surgery chemotherapy.
  • People whose tumor cells have been confirmed to show expression of a protein called AXL, based on a laboratory tissue test.
  • People who can provide tumor tissue samples — both a recent sample (taken after the most recent cancer progression or relapse) and, if available, an older archived sample from before that progression.
  • People who have at least one measurable tumor that can be assessed using standard imaging criteria (RECIST 1.1).
  • People with a functional status score of 0 or 1 on the ECOG scale, meaning they are fully active or able to carry out light activity (confirm with trial site).
  • People who, in the trial doctor's opinion, have a life expectancy of at least 4 months from the time of signing the consent form.

Who may not be able to join:

  • People for whom a curative surgery or full-course radiotherapy is considered appropriate, unless it is minor surgery or palliative (comfort-focused) radiation.
  • People with currently active cancer spread to the brain or the lining of the brain and spinal cord. People with previously treated brain metastases may still be considered if the metastases were treated with surgery or radiation, have been stable for at least 4 weeks before joining the study (meaning no neurological symptoms, no need for steroid medications, and no individual lesion larger than 1.5 cm), and show no signs of new or worsening brain involvement. People newly found to have brain metastases during the screening period are not eligible.

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
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Arina V Zinkina-Orikhan, PhD, Director of Clinical Development Department, BIOCAD

Phone: +7 911 081 23 68

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
Phase 2
Sponsor
Biocad
Registry
ClinicalTrials.gov
Start date
15 July 2024
Est. completion
1 December 2025

Where this trial is recruiting

Belarus 🇷🇺 Russia

Primary endpoints

Overall response rate (ORR)

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