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Clinical Trials in India / NCT07680790
Starting soon Phase 3

Study of Izalontamab Brengitecan (BMS-986507) in Combination With Osimertinib Versus Osimertinib Monotherapy or Osimertinib in Combination With Platinum-based Chemotherapy for EGFRmt Non-small Cell Lung Cancer (IZABRIGHT-Lung02)

NCT07680790 · tracked via the Priya Life Science India tracker
Sponsor
Bristol-Myers Squibb
Phase
Phase 3
Started
2026-09-30
Last updated
2026-08-24

Condition(s) studied

Non-Small Cell Lung Cancer

Investigational drug(s) / intervention(s)

Iza-brenOsimertinibPemetrexedCarboplatinCisplatin

Iza-bren: Specified dose on specified days

Osimertinib: Specified dose on days

Pemetrexed: Specified dose on specified days

Carboplatin: Specified dose on specified days

Cisplatin: Specified dose on specified days

Study summary

The purpose of this study is to evaluate izalontamab brengitecan (iza-bren) combined with osimertinib in participants with previously untreated, locally advanced or metastatic EGFR-mutant NSCLC, compared to osimertinib alone or osimertinib combined with platinum-based chemotherapy

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Participants must have histologically or cytologically confirmed non-squamous NSCLC, newly diagnosed locally advanced (Stage IIIB/IIIC), metastatic (Stage IVA/IVB), or recurrent disease not amenable to curative surgery or definitive radiotherapy and requiring systemic treatment * Participants must have documented EGFR-TKI-sensitizing mutation (exon 19 deletion or exon 21 L858R substitution) * Participants must have measurable extracranial disease per RECIST v1.1 as assessed by the investigator * Participants must have ECOG Performance Status 0-1 Exclusion Criteria: * Participants must not have unstable, symptomatic, or uncontrolled CNS metastases, including brain, leptomeningeal disease, and/or spinal cord compression * Participants must not have history of ILD/pneumonitis requiring treatment with steroids (≥ Grade 2), or current or suspected ILD/pneumonitis * Participants must not have clinically significant cardiac disease * Other protocol-defined inclusion/exclusion criteria apply.

Primary outcome measure(s)

Trial sites (208)

FacilityCityRegionStatus
Local Institution - 0212 Beverly Hills California
Local Institution - 0504 Fullerton California
Local Institution - 0357 La Jolla California
Local Institution - 0520 Pueblo Colorado
Local Institution - 0527 Fort Myers Florida
Local Institution - 0366 Orlando Florida
Local Institution - 0519 Palm Bay Florida
Local Institution - 0526 St. Petersburg Florida
Local Institution - 0524 West Palm Beach Florida
Local Institution - 0210 Honolulu Hawaii
Local Institution - 0207 Ottawa Illinois
Local Institution - 0503 Baltimore Maryland
Local Institution - 0523 Silver Spring Maryland
Local Institution - 0521 Edina Minnesota
Local Institution - 0364 Saint Paul Minnesota
Local Institution - 0403 St Louis Missouri
Local Institution - 0402 Omaha Nebraska
Local Institution - 0290 Lebanon New Hampshire
Local Institution - 0183 New Brunswick New Jersey
Local Institution - 0153 New York New York
Local Institution - 0157 The Bronx New York
Local Institution - 0385 Charlotte North Carolina
Local Institution - 0438 Sandusky Ohio
Local Institution - 0404 Portland Oregon
Local Institution - 0487 Easton Pennsylvania
Local Institution - 0200 Sioux Falls South Dakota
Local Institution - 0199 Memphis Tennessee
Local Institution - 0522 Beaumont Texas
Local Institution - 0525 Dallas Texas
Local Institution - 0529 San Antonio Texas
Local Institution - 0411 Salt Lake City Utah
Local Institution - 0165 Fairfax Virginia
Local Institution - 0530 Fairfax Virginia
Local Institution - 0528 Winchester Virginia
Local Institution - 0283 Seattle Washington
Local Institution - 0502 Morgantown West Virginia
Local Institution - 0077 Mar del Plata Buenos Aires
Local Institution - 0514 Río Cuarto Córdoba Province
Local Institution - 0086 Buenos Aires Argentina
Local Institution - 0432 Buenos Aires Argentina

+ 168 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07680790 on ClinicalTrials.gov ↗ ← All trials in India