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Taking people in SwitzerlandPhase 2/3

Tests izalontamab brengitecan against chemotherapy in lung cancer after EGFR drug failure

Tests izalontamab brengitecan against platinum chemotherapy in adults with EGFR-mutated lung cancer.

Plain-language title generated from the registry record
Registry title: Study of Izalontamab Brengitecan (BMS-986507) Versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer After Failure of EGFR TKI Therapy (IZABRIGHT-Lung01)

Key facts

Where
Baden, Bellinzona, and Sankt Gallen, SwitzerlandSee the 3 sites
Phase
Phase 2/3

Where in Switzerland

  • Kantonsspital BadenBaden, SwitzerlandTaking people
  • BellinzonaBellinzona, SwitzerlandNot yet recruiting
  • Cantonal Hospital St GallenSankt Gallen, SwitzerlandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Bristol-Myers Squibb
Trial code
NCT07100080
Record updated
9 October 2026
Original description
A Study of Izalontamab Brengitecan (BMS-986507) versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer after failure of EGFR TKI TherapyRead full original descriptionShow less

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

A Study of Izalontamab Brengitecan (BMS-986507) versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer after failure of EGFR TKI Therapy

Inclusion: Non-squamous NSCLC, not amenable to treatment in curative intent; Documented evidence of EGFR mutation (exon 19 deletion, L858R mutation); Progressive disease on a 3rd-generation (such as osimertinib, furmonertinib, lazertinib,...) EGFR-TKI-based mono- or combination therapy regimen as the most recent line of therapy in an adjuvant, locally advanced, or metastatic treatment setting; Eligible to receive a platinum-based doublet chemotherapy regimen (either cisplatin or carboplatin in combination with pemetrexed).

Exclusion: Poorly controlled systemic medical conditions; Inadequate organ function and/or bone marrow reserve; Leptomeningeal metastases or spinal cord compression; Other protocol-defined inclusion/exclusion criteria apply.

ClinicalTrials.gov NCT07100080