A Study of Izalontamab Brengitecan Versus Chemotherapy in Participants With Previously Untreated, Locally Advanced, Recurrent Inoperable, or Metastatic Triple-negative Breast Cancer Ineligible for Anti-PD(L)1 Drugs (IZABRIGHT-Breast01)

Sponsor: Bristol-Myers Squibb

Sponsor score: 60

ClinicalTrials ID:NCT06926868

This study evaluates the efficacy and safety of iza-bren, a bi-specific antibody-drug conjugate, compared to standard chemotherapy options in patients with advanced TNBC or ER-low, HER2-negative BC ineligible for anti-PD(L)1 therapies. Eligible participants must have measurable disease and no prior systemic therapy in the incurable setting. Interventions include iza-bren, nab-paclitaxel, paclitaxel, capecitabine, carboplatin, and gemcitabine.

Patient Parameters

Program Overview

The purpose of this study is to assess the efficacy and safety of iza-bren, a bi-specific antibody-drug conjugate against EGFR and HER3 with a topoisomerase inhibitor payload versus treatment of physician's choice (TPC) (paclitaxel, nab-paclitaxel, carboplatin plus gemcitabine, and capecitabine) for the treatment of first-line metastatic triple-negative breast cancer (TNBC) or estrogen receptor (ER)-low, human epidermal growth factor receptor 2 (HER2)-negative BC patients who are not candidates for anti-PD(L)1 therapy and endocrine therapies.

Eligibility Criteria

Inclusion Criteria

  • Histologically or cytologically confirmed and documented locally-advanced, recurrent inoperable, or metastatic TNBC (ER < 1%, PgR < 1%, HER2 IHC 0, 1+, or 2+ with FISH negative for HER2 gene amplification) or ER-low, HER2-negative BC (ER and / or PgR 1% to 10%, HER2 IHC 0, 1+, or 2+ with FISH negative for HER2 gene amplification) per ASCO/CAP criteria, based on the most recently analyzed biopsy or other pathology specimen.
  • Patients with recurrent disease must have experienced disease relapse at least 6 months after finishing their last therapy with curative intent.
  • Patients with TNBC must be considered ineligible for 1L chemotherapy combination treatment with an anti-PD-1 or an anti-PD-L1 due to either one of the following criteria:.
  • Investigator-determined ineligibility based on PD-L1 negative disease determined and documented prior to trial screening as part of SoC.
  • Has experienced disease relapse between 6 to 12 months after the completion of (neo)adjuvant therapy with an anti-PD(L)1.
  • Has a severe auto-immune disease or other contraindication.
  • Patients with ER-low, HER2-negative BC must be ineligible, in the opinion of the Investigator, for endocrine therapy-based treatments.
  • No previous systemic therapy in the locally advanced, recurrent inoperable or metastatic setting (ie incurable setting).
  • Measurable disease by CT or MRI as per RECIST v1.1.
  • Other protocol-defined Inclusion/Exclusion criteria apply.

Locations

FACILITYZIPCITYSTATE
Local Institution - 030371913Hot SpringsArkansas
Local Institution - 030790703CerritosCalifornia
Local Institution - 030890703CerritosCalifornia
Local Institution - 030990703CerritosCalifornia
Local Institution - 031190805Long BeachCalifornia
Local Institution - 029090033Los AngelesCalifornia
Local Institution - 028390067Los AngelesCalifornia
Local Institution - 028980045AuroraColorado
Local Institution - 030419713NewarkDelaware
Local Institution - 028233136MiamiFlorida

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