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

Description

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

Conditions

Non-Small Cell Lung Cancer

Study Overview

Study Details

Study overview

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

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 (TPS ≥ 50%)

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

Condition
Non-Small Cell Lung Cancer
Intervention / Treatment

-

Contacts and Locations

Cerritos

Summit Therapeutics Research Center, Cerritos, California, United States, 90703

Los Angeles

Summit Therapeutics Research Center, Los Angeles, California, United States, 90067

Tamarac

Summit Therapeutics Research Center, Tamarac, Florida, United States, 33321

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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.
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Summit Therapeutics,

Study Record Dates

2029-06