Clinical Trial

Trial Protocol ID USOR 23208: Heavily pretreated MBC

Trial Description

A Randomized, Open-label Study Comparing the Bria IMT Regimen in Combination with Check Point Inhibitor vs Physician’s Choice in Metastatic Breast Cancer (BRIA-ABC)

MOA: A Randomized, Open-label Study Comparing the Bria IMT Regimen in Combination with Check Point Inhibitor vs Physician’s Choice in Metastatic Breast Cancer (BRIA-ABC)

Key Eligibility:

  • MBC that have failed prior tx and have no meaningful alternative tx available
    • HER2+: ≥3 prior tx with ≥2 anti-HER2 and ≥1 chemotherapy regiment
    • ER+/PR+: refractory to hormonal tx (PD on ≥2 agents, in 2 separate lines)
    • TNBC: must have exhausted all curative intent tx including ≥2 prior chemo (neo and/or adjuvant settings)
    • Known germline/genomic actionable targets: must have had all tumor directed indicated tx
    • HER2-low: ≥HER2-targeted agent approved HER2-low in addition to any HR tx or germline/genomic actionable targets tx
    • HER2-negative: refractory to HR tx (if indicated) and had ≥2 prior chemotherapy
    • New or progressive BC metastatic to the brain are eligible if clinically stable, does not require steroid or had it discontinued ≥2 weeks prior to the first dose, and ≥3 weeks since surgical debulking before first dose
    • ECOG: 0-2

Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724

Investigator

  • Photo of Nadia Ashai, MD Nadia Ashai, MD

Disease Types

ClinicalTrials.gov NCT ID

  • NCT06072612