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Clinical Trial Summary

PUMA-ALI-1201 is a randomized, dose optimization, multicenter, Phase 2 study of alisertib administered in combination with endocrine therapy in participants with pathology-confirmed HR-positive/HER2-negative metastatic breast cancer (MBC) following progression on or after at least two prior lines of endocrine therapy in the recurrent or metastatic setting. This study is intended to evaluate the optimal alisertib dose administered in combination with the selected endocrine therapy. The study is also planned to evaluate the efficacy, safety, and pharmacokinetics of alisertib in combination with endocrine and to identify the biomarker-defined subgroup(s) that may benefit most from combined alisertib and endocrine therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06369285
Study type Interventional
Source Puma Biotechnology, Inc.
Contact Puma Biotechnology, Inc. Clinical Operations Senior Director
Phone 424-248-6500
Email ClinicalTrials@pumabiotechnology.com
Status Not yet recruiting
Phase Phase 2
Start date December 31, 2024
Completion date December 31, 2028

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