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Izalontamab Brengitecan · BMS-986507

Bispecific antibody · Cytotoxic, directed at EGFR and HER3 (ERBB3) · developed by BRISTOL MYERS SQUIBB

Phase 2/3 Most advanced trial
BMY Developer
2 Registered trials

What is Izalontamab Brengitecan?

Izalontamab brengitecan is a bispecific antibody-drug conjugate targeting EGFR and HER3, conjugated to Ed-04, a topoisomerase 1 inhibitor. Upon binding to EGFR and HER3 on cancer cells and internalization, Ed-04 is released to inhibit DNA topoisomerase I, causing cell cycle arrest and apoptosis. It is studied in lung cancer and breast cancer.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
BMS-986507, Iza-bren
Drug type
Bispecific antibody
Targets
EGFR, HER3 (ERBB3), DNA topoisomerase I (TOP1) (secondary target)
Mechanism
Cytotoxic, directed at EGFR and HER3 (ERBB3)
Pathways
DNA replication inhibition, apoptosis
Therapy area
Oncology
Developer
BRISTOL MYERS SQUIBB (BMY)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 2/3
UNII
UC2FX6YY3P

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT07100080 Phase 2/3 Non-Small Cell Lung Cancer Recruiting BMY
NCT06618287 Phase 1/2 Lung Cancer Recruiting BMY

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Breast CancerLung CancerNon-Small Cell Lung Cancer

Other drugs acting on EGFR / ERBB3

More from BRISTOL MYERS SQUIBB

Sources

Updated Oct 3, 2026. Something wrong or missing? Report it on the BMY page.

Follow BMY, the company behind Izalontamab Brengitecan

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.