A Global Study of Volrustomig (MEDI5752) Plus Chemotherapy Versus Pembrolizumab Plus Chemotherapy for Participants With Metastatic Non-small Cell Lung Cancer.
The purpose of eVOLVE-Lung02 is to test the effectiveness (efficacy) and measure the safety of volrustomig in combination with chemotherapy compared with pembrolizumab in combination with chemotherapy as 1L treatment in participants with mNSCLC in PD-L1 \< 50%.
Checked against the public recordLast updated Jul 28, 2026 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 3
- Sponsor
- AstraZeneca
- Interventions being studied
- Drug: Volrustomig; Drug: Pembrolizumab; Drug: Carboplatin; Drug: Paclitaxel; Drug: Pemetrexed
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Key Inclusion Criteria: * Histologically or cytologically documented squamous or non-squamous NSCLC. * Stage IV NSCLC (according to Version 8 of the IASLC Staging Manual in Thoracic Oncology 2016), not amenable to curative surgery or radiation. * Absence of sensitizing EGFR mutations and ALK and ROS1 rearrangements. * Absence of documented tumor genomic alteration results from tests conducted as part of standard local practice in any other actionable driver oncogenes for which there are locally approved targeted first-line therapies. Key Exclusion Criteria: * Mixed small-cell lung cancer and NSCLC histology or sarcomatoid variant. Rare subtypes are excluded. * Spinal cord compression. * Symptomatic brain metastases. Brain metastases may be treated or untreated, but participants must be asymptomatic and off steroids for at least 14 days prior to start of study intervention. A minimum of 2 weeks must have elapsed between the end of brain radiotherapy and study enrollment. * History of another primary malignancy except for: 1. Malignancy treated with curative intent with no known active disease ≥ 2 years before the first dose of study intervention and of low potential risk for recurrence. 2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease. 3. Adequately treated carcinoma in situ without evidence of disease. * As judged by the investigator, any condition that would interfere with evaluation of the study intervention or interpretation of participant safety or study results.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Research SiteHot Springs, Arkansas
- Research SiteSpringdale, Arkansas
- Research SiteLong Beach, California
- Research SiteLone Tree, Colorado
- Research SiteFort Myers, Florida
- Research SiteOrlando, Florida
- Research SiteSt. Petersburg, Florida
- Research SiteWest Palm Beach, Florida
- Research SiteFort Wayne, Indiana
- Research SiteIndianapolis, Indiana
- Research SiteDes Moines, Iowa
- Research SiteLexington, Kentucky
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 28, 2026. Always confirm current availability with the study team.