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
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
| Parameter | Options |
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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
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Local Institution - 0303 | 71913 | Hot Springs | Arkansas |
| Local Institution - 0307 | 90703 | Cerritos | California |
| Local Institution - 0308 | 90703 | Cerritos | California |
| Local Institution - 0309 | 90703 | Cerritos | California |
| Local Institution - 0311 | 90805 | Long Beach | California |
| Local Institution - 0290 | 90033 | Los Angeles | California |
| Local Institution - 0283 | 90067 | Los Angeles | California |
| Local Institution - 0289 | 80045 | Aurora | Colorado |
| Local Institution - 0304 | 19713 | Newark | Delaware |
| Local Institution - 0282 | 33136 | Miami | Florida |
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