Phase 2 Breast Cancer Trial, Recruiting NCT07208149 Sponsor: Shenzhen Majory Biotechnology Co., Ltd. Condition: Breast Cancer
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Phase 2 Breast Cancer Trial, Recruiting

NCT07208149
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 been diagnosed with triple-negative breast cancer (a specific type of breast cancer) confirmed through a lab test on a tissue or cell sample.
  • People whose triple-negative breast cancer has come back in the same area or spread to other parts of the body, and has continued to grow after at least one previous cancer treatment.
  • People who have at least one tumour that can be measured on a scan, according to standard measurement guidelines.
  • People who are either fully active or have mild limits on physical activity but are still able to do light work (confirm with trial site what this means for individual circumstances).
  • People who are expected to live for more than 3 months.
  • People whose blood tests show that their organs and blood cell levels are working well enough to participate.
  • People who are willing to read and sign a consent form agreeing to take part.

Who may not be able to join:

  • People who have had a serious allergic reaction to similar medicines in the past, including antibody-based treatments, or who have a medical reason they cannot take the study drug.
  • People who need to take medicines that suppress the immune system across the whole body, either within 14 days before starting the trial or during the trial.
  • People who have had major surgery (not including minor procedures like needle biopsies) within 4 weeks before starting the trial, or who are expected to need major surgery during the trial.
  • People who have cancer that has spread to the brain or the lining around the brain and spine, and is not currently under control.
  • People who have a history of an autoimmune disease that has required treatment with steroids or immune-suppressing medicines.
  • People who are trying to become pregnant, are currently pregnant, or are breastfeeding.
  • People where the trial doctor believes participation may create additional health risks or affect the reliability of the trial results.

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 21 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: Binghe Xu, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: +86 13332895357

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
Shenzhen Majory Biotechnology Co., Ltd.
Registry
ClinicalTrials.gov
Start date
29 January 2026
Est. completion
1 September 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of participants who experience one or more dose-limiting toxicities (DLTs); Maximum Tolerated Dose (MTD) of MR001; Incidence of Adverse Events (AEs) as Assessed by CTCAE v5.0

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: 21 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