Study of ECI830 Single Agent or in Combination in Patients With Advanced HR+/HER2- Breast Cancer and in Patients With Other Advanced Solid Tumors
Sponsored by Novartis Pharmaceuticals
About this study
Phase I: Characterize safety and tolerability of ECI830 as a single agent and in combination with ribociclib and fulvestrant. Identify dose range for optimization/recommended dose for future studies. Phase II: Assess the anti-tumor activity of ECI830 in combination with ribociclib and fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer.
Enrolling at this location
Fred Hutch Cancer Research
Seattle, Washington
I'm interestedThis study also enrolls at 7 other locations. See all.
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Trial data sourced from ClinicalTrials.gov.