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Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients With High PD-L1

RecruitingPhase 3

A Randomized, Double-blinded, Multiregional Phase 3 Study of Ivonescimab Versus Pembrolizumab for the First-line Treatment of Metastatic Non-small Cell Lung Cancer in Patients Whose Tumors Demonstrate High PD-L1 Expression

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age ≥ 18 years old at the time of enrollment
* Eastern Cooperative Oncology Group (ECOG) performance status score of 0 - 1
* Expected life expectancy ≥ 3 months
* Metastatic (Stage IV) NSCLC
* Histologically or cytologically confirmed squamous or non-squamous NSCLC
* Tumor demonstrates high PD-L1 expression ( TPS\>50%) based on a 22C3 immunohistochemistry ( IHC) clinical assay approved / cleared by local health authorities.
* At least one measurable noncerebral lesion according to RECIST 1.1
* No prior systemic treatment for metastatic NSCLC.

Exclusion Criteria:

* Histologic or cytopathologic evidence of the presence of small cell lung carcinoma for which first-line approved therapies are indicated. For patients with non-squamous histology, actionable driver mutation testing results are required before randomization.
* Has received any prior therapy for NSCLC in the metastatic setting.
* Concurrent enrollment in another clinical study, unless patient is enrolled in a non-interventional clinical study or is completing survival follow -up.
* Known actionable genomic alterations for which first-line approved therapies are indicated
* Symptomatic CNS metastases, CNS metastasis ≥ 1.5 cm, CNS radiation within 7 days prior to randomization, potential need for CNS radiation within the first cycle, or leptomeningeal disease
* Other prior malignancy (including previously treated NSCLC) unless the patient has undergone curative therapy with no evidence of recurrence of the disease for 3 years prior to randomization
* Active autoimmune or lung disease requiring systemic therapy
* Has pre-existing peripheral neuropathy that is ≥ Grade 2 by CTCAE version 5
* Severe infection within 4 weeks prior to randomization
* Major surgical procedures or serious trauma within 4 weeks prior to randomization
* History of noninfectious pneumonia requiring systemic corticosteroids, or current interstitial lung disease

About the study

Clinical study of ivonescimab for first-line treatment of metastatic NSCLC patients with high PD-L1. Evaluating overall survival and progression free survival.

What is being tested

Sponsor: Summit Therapeutics · Participants: 780 · Started: Feb 27, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06767514

Locations in the U.S.

ArizonaClinical Study Site, Chandler
Clinical Study Site, Phoenix
ArkansasClinical Study Site, Hot Springs
Clinical Study Sites, Jonesboro
CaliforniaClinical Study Site, Alameda
Clinical Study Site, Anaheim
Clinical Study Site, Beverly Hills
Clinical Study Site, Cerritos
Clinical Study Site, Los Angeles
Clinical Study Site, Los Angeles
Clinical Study Site, Orange
Clinical Study Site, Oxnard
Clinical Study Site, San Diego
Clinical Study Site, Sunnyvale
Clinical Study Site, Torrance
ColoradoClinical Study Site, Aurora
Clinical Study Site, Denver
Clinical Study Site, Grand Junction
Clinical Study Site, Lone Tree
Clinical Study Site, Loveland
FloridaClinical Study Site, Fort Lauderdale
Clinical Study Sites, Fort Lauderdale
Clinical Study Site, Jacksonville
Clinical Study Site, Jacksonville Beach
Clinical Study Site, North Venice
Clinical Study Site, Ocala
Clinical Study Site, Orlando
Clinical Study Site, Pensacola
Clinical Study Site, Plantation
Clinical Study Site, St. Petersburg
Clinical Study Site, Tallahassee
Clinical Study Site, Tamarac
Clinical Study Site, West Palm Beach
GeorgiaClinical Study Site, Atlanta
Clinical Study Site, Warner Robins
IllinoisClinical Study Site, Carterville
Clinical Study Site, Chicago
Clinical Study Site, Chicago
Clinical Study Site, Evanston
IndianaClinical Study Site, Indianapolis
IowaClinical Study Site, Waukee
KentuckyClinical Study Site, Lexington
LouisianaClinical Study Site, Covington
MarylandClinical Study Site, Baltimore
MassachusettsClinical Study Site, Boston
Clinical Study Site, Brighton
Clinical Study Site, Foxborough
Clinical Study Site, Methuen
Clinical Study Site, Milford
Clinical Study Site, Weymouth
Clinical Study Site, Worcester
MichiganClinical Study Site, Ann Arbor
Clinical Study Site, Detroit
Clinical Study Sites, Detroit
MinnesotaClinical Study Sites, Duluth
Clinical Study Site, Minneapolis
Clinical Study Site, Saint Paul
MississippiClinical Study Site, Hattiesburg
MissouriClinical Study Site, Kansas City
Clinical Study Site, St Louis
Clinical Study Site, St Louis
New HampshireClinical Study Site, Lebanon
New JerseyClinical Study Site, Mullica Hill
Clinical Study Site, New Brunswick
New YorkClinical Study Site, New York
Clinical Study Site, Syracuse
Clinical Site, The Bronx
North CarolinaClinical Study Site, Chapel Hill
Clinical Study Site, Durham
Clinical Study Site, Pinehurst
OhioClinical Study Sites, Cincinnati
Clinical Study Site, Cleveland
Clinical Study Site, Columbus
Clinical Study Sites, Columbus
OklahomaClinical Study Site, Oklahoma City
OregonClinical Study Site, Eugene
Clinical Study Site, Portland
PennsylvaniaClinical Study Site, Philadelphia
Clinical Study Site, Pittsburgh
South CarolinaClinical Study Site, Greenville
TennesseeClinical Study Site, Nashville
Clinical Study Sites, Nashville
TexasClinical Study Site, Abilene
Clinical Study Site, Austin
Clinical Study Site, Dallas
Clinical Study Site, Fort Worth
Clinical Study Site, Houston
Clinical Study Site, Tyler
Clinical Study Site, Webster
UtahClinical Study Site, Salt Lake City
VirginiaClinical Study Site, Blacksburg
Clinical Study Site, Charlottesville
Clinical Study Site, Fairfax
Clinical Study Site, Richmond
Clinical Study Site, Richmond
WashingtonClinical Study Site, Seattle
Clinical Study Site, Vancouver

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.