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NCT Number: NCT06926868

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)

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Local Institution - 0011, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 ISH 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 ISH 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:

i) Investigator-determined ineligibility based on PD-L1 negative disease determined and documented prior to trial screening as part of SoC; ii) Has experienced disease relapse between 6 to 12 months after the completion of (neo)adjuvant therapy with an anti-PD(L)1; iii) 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.

Treatment and study plan

Iza-bren

Drug

Specified dose on specified days

Other names: BMS-986507, BL-B01D1, Izalontamab brengitecan

Nab-paclitaxel

Drug

Specified dose on specified days

paclitaxel

Drug

Specified dose on specified days

Capecitabine

Drug

Specified dose on specified days

carboplatin

Drug

Specified dose on specified days

Gemcitabine

Drug

Specified dose on specified days

Primary outcomes

  1. Progression-Free Survival (PFS)

    Time frame: Approximately 31 months from first participant randomization

    Assessed using Response Evaluation Criteriain Solid Tumors version 1.1 (RECIST v1.1) byblinded independent central review (BICR)

Secondary outcomes

  1. Overall Survival (OS)

    Time frame: Approximately up to 57 months from first participant randomization

  2. Recommended Phase 3 Dose (RP3D) of BMS-986507

    Time frame: Approximately 19 months from first participant randomization

  3. Number of participants with treatment-related Adverse Events (AEs)

    Time frame: Approximately up to 57 months from first participant randomization

  4. Number of participants with laboratory abnormalities

    Time frame: Approximately up to 57 months from first participant randomization

  5. Number of participants with serious AEs (SAEs)

    Time frame: Approximately up to 57 months from first participant randomization

  6. Number of participants with AEs leading to treatment discontinuation, interruption, dose reduction or dose delay

    Time frame: Approximately up to 57 months from first participant randomization

  7. Number of deaths

    Time frame: Approximately up to 57 months from first participant randomization

  8. Objective Response (OR)

    Time frame: Approximately 31 months from first participant randomization

  9. PFS rate

    Time frame: Approximately 19 months from first participant randomization

    Assessed using RECIST v1.1 by BICR

  10. PFS

    Time frame: Approximately 31 months from first participant randomization

    Assessed by Investigator

  11. Disease control rate (DCR)

    Time frame: Approximately 31 months from first participant randomization

  12. Duration of Response (DOR)

    Time frame: Approximately 31 months from first participant randomization

  13. Time to Response (TTR)

    Time frame: Approximately 31 months from first participant randomization

  14. Time to subsequent treatment (TTST)

    Time frame: Approximately up to 57 months from first participant randomization

    Defined as time from randomization to the start of subsequent therapy or death

  15. Progression-free survival after next line of treatment (PFS2)

    Time frame: Approximately up to 57 months from first participant randomization

    Defined as the time from randomization to the date of investigator-defined documented disease progression after next line of treatment or death due to any cause, whichever comes first

  16. Change from baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)

    Time frame: Approximately up to 57 months from first participant randomization

  17. Change from baseline in EORTC Breast Cancer-specific Quality of Life Questionnaire (QLQ-BR23)

    Time frame: Approximately up to 57 months from first participant randomization

  18. Functional Assessment of Chronic Illness Therapy item GP5 (FACIT GP5) score

    Time frame: Approximately up to 57 months from first participant randomization

  19. Change from baseline in European Quality of Life 5 Dimensions 5 Levels (EQ-5D-5L)

    Time frame: Approximately up to 57 months from first participant randomization

  20. Relative change in tumor size

    Time frame: Approximately up to 19 months from first participant randomization

  21. ORR by RECIST v1.1 per Investigator

    Time frame: Approximately 31 months from first participant randomization

Study contacts

Contact information is provided by the study sponsor or research team.

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

CONTACT

[email protected]

855-907-3286

First line of the email MUST contain NCT # and Site #.

CONTACT

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Collaborators

  • SystImmune Inc.

Registry information

Official study title

IZABRIGHT-Breast01: A Randomized, Open-label, Inferentially Seamless Phase 2/3 Study of Izalontamab Brengitecan (BMS-986507) Versus Treatment of Physician's Choice in Patients With Previously Untreated, Locally Advanced, Recurrent Inoperable, or Metastatic Triple-negative Breast Cancer (TNBC) or ER-low, HER2-negative BC Who Are Ineligible for Anti-PD1/PD-L1 Treatment

Important dates

Study start
2025
Primary completion
2028
Study completion
2030
First posted
Apr 15, 2025
Registry last updated
Jun 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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