A Phase 1 Study of 68Ga-R11228 and 177Lu-R11228 in Breast Cancer (NCT07121244) | Clinical Trial Compass
TerminatedPhase 1
A Phase 1 Study of 68Ga-R11228 and 177Lu-R11228 in Breast Cancer
Stopped: Sponsor decision
United States, Australia11 participantsStarted 2025-10-01
Plain-language summary
A phase 1 study of 68Ga-R11228 and 177Lu-R11228 in breast cancer.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Part A
* Pathologically confirmed estrogen and/or progesterone receptor (ER/PR) positive and HER2 negative locoregionally recurrent or metastatic breast cancer
* At least one target or non-target lesion per RECIST v1.1 criteria.
* Male or non-pregnant, non-lactating female subjects age ≥18 years.
Part B
* Pathologically confirmed estrogen and/or progesterone receptor (ER/PR) positive and HER2 negative locoregionally recurrent or metastatic breast cancer
* Refractory to endocrine therapy. Note: there is no limit on prior number of lines of endocrine therapy or prior treatments with CDK4/6, AKT, PI3K and/or mTOR inhibitors.
* Received or declined at least one line of chemotherapy or antibody drug conjugate in the locoregionally recurrent or metastatic setting
* Progressive disease or intolerance to last treatment.
* At least one target lesion per RECIST v1.1 criteria.
* Male or non-pregnant, non-lactating female subjects age ≥18 years.
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
* Life expectancy of at least six months.
* Adequate bone marrow reserve, hepatic function and renal function.
Exclusion Criteria:
Part A
* Study participant has not recovered from clinically significant adverse event(s) resulting from most recent anticancer therapy/intervention.
* Known central nervous system (CNS) disease, except for those subjects with treated brain metastasis who are stable for at least 1 month, having no evidence of progressi…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Incidence of adverse events [68Ga-R11228]
Timeframe: Day 1 to Day 7
2
Incidence of Serious Adverse Events [68Ga-R11228]
Timeframe: Day 1 to Day 7
3
Incidence of adverse events [177Lu-R11228]
Timeframe: Day 1 to week 36
4
Incidence of Serious Adverse Events [177Lu-R11228]
Timeframe: Day 1 to week 36
5
Incidence of dose limiting toxicities [177Lu-R11228]