This phase I/II trial studies the side effects and best dose of copanlisib and how well it works when given together with eribulin in treating patients with triple negative breast cancer that has spread from where it first started (primary site) to other places in the body (metastatic). Copanlisib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Chemotherapy drugs, such as eribulin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving copanlisib and eribulin together may work better in treating advanced stage triple negative breast cancer compared to eribulin alone.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
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.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Maximum Tolerated Dose of Eribulin (MTD) (Phase I)
Timeframe: Up to 28 days
Recommended Phase 2 Dose of Eribulin (RP2D) (Phase I)
Timeframe: Up to 28 days
Maximum Tolerated Dose of Copanlisib (MTD) (Phase I)
Timeframe: Up to 28 days
Recommended Phase 2 Dose of Copanlisib (RP2D) (Phase I)
Timeframe: Up to 28 days
Progression Free Survival (PFS) (Phase II)
Timeframe: From date of treatment start to date of progression or death, assessed up to 36 months