Zunsemetinib in Combination With Capecitabine in Patients With Hormone Receptor-Positive and HER2-Negative Metastatic Breast Cancer With Bone Metastasis

This is a phase Ib/II study evaluating the safety and efficacy of zunsemetinib (ATI-450) with capecitabine in patients with hormone receptor-positive and HER2-negative (HR+/HER2-) metastatic breast cancer (MBC).

Trial Details

NCT ID
NCT06374459
Phase
PHASE1 / PHASE2
Sponsor
Washington University School of Medicine
Status
RECRUITING
Cancer Type
ER/PR Positive (Hormone Receptor Positive) Breast Cancer
Interventions
  • Zumsemetinib
  • Capecitabine
  • Zoledronic acid
  • Denosumab
Locations (sample)
  • Westwood, Kansas, United States|39.04056,-94.6169
  • Rochester, Minnesota, United States|44.02163,-92.4699
  • St Louis, Missouri, United States|38.62727,-90.19789

Key Eligibility Criteria

  • Hormone receptor-positive, HER2-negative metastatic breast cancer.
  • Measurable or non-measurable but evaluable disease by RECIST v1.1.
  • Candidate for capecitabine treatment per physician decision. See below phase-specific eligibility criteria for further guidance.
  • No more than one prior chemotherapy for metastatic disease.

For full eligibility, visit ClinicalTrials.gov.

Check If You May Be Eligible

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