Iza-bren
DrugSpecified dose on specified days
Other names: BMS-986507, BL-B01D1, Izalontamab brengitecan
NCT Number: NCT07100080
A Study of Izalontamab Brengitecan (BMS-986507) versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer after failure of EGFR TKI Therapy
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Instituto Alexander Fleming, 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
Exclusion criteria
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
Time frame: Approximately 3 months after the first dose
Phase 2
Time frame: Up to 3 years
Phase 3
Time frame: Up to 3 years
Phase 2
Time frame: Up to 3 years
Phase 2
Time frame: Up to 5 years
Phase 3
Time frame: Up to 3 years
Phase 3
Time frame: Up to 3 years
Phase 3
Time frame: Up to 3 years
Phase 3
Time frame: Up to 3 years
Phase 3
Time frame: Up to 3 years
Phase 3
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-Lung01: A Randomized, Open-label, Phase 2/3 Study of Izalontamab Brengitecan (BMS-986507) Versus Platinum-based Chemotherapy in Patients With EGFR-mutated Non-small Cell Lung Cancer and Disease Progression on EGFR Tyrosine Kinase Inhibitor Therapy
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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