Phase 3 Breast Cancer Trial, Recruiting
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:
- You are a woman aged 18 or older
- You have been diagnosed with HER2-positive breast cancer, confirmed through a laboratory test on a tissue sample
- You are expected to receive a treatment plan that includes a drug called pyrotinib, either before surgery or for breast cancer that has spread or cannot be removed
- You have received no more than one previous HER2-targeted treatment for cancer that has come back or spread
- You are able to use a mobile phone and read on your own
- The trial doctor has assessed that you are in a suitable mental and physical condition to take part
Who may not be able to join:
- You have a history of cognitive impairment (problems with memory or thinking)
- You have severe problems with your vision or hearing
- You have taken pyrotinib before
- You are pregnant, breastfeeding, or planning to become pregnant
- You have tried a talking-based therapy (such as cognitive-behavioral therapy) in the past year that did not help (confirm with trial site)
- You have taken part in another clinical trial in the month before being assessed for this study
- The trial doctor has decided that your mental or physical condition makes participation unsuitable
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
medication adherence at 1-year
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.