Iza-bren
DrugSpecified dose on specified days
Other names: BMS-986507, BL-B01D1, Izalontamab brengitecan
NCT Number: NCT06926868
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Local Institution - 0011, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion 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.
Specified dose on specified days
Other names: BMS-986507, BL-B01D1, Izalontamab brengitecan
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
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)
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately 19 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately 31 months from first participant randomization
Time frame: Approximately 19 months from first participant randomization
Assessed using RECIST v1.1 by BICR
Time frame: Approximately 31 months from first participant randomization
Assessed by Investigator
Time frame: Approximately 31 months from first participant randomization
Time frame: Approximately 31 months from first participant randomization
Time frame: Approximately 31 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Defined as time from randomization to the start of subsequent therapy or death
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
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 57 months from first participant randomization
Time frame: Approximately up to 19 months from first participant randomization
Time frame: Approximately 31 months from first participant randomization
Contact information is provided by the study sponsor or research team.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
CONTACT
First line of the email MUST contain NCT # and Site #.
CONTACT
Bristol-Myers Squibb
Industry
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
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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