Clinical Trial

A Multiple Antigen Vaccine (STEMVAC) for the Treatment of Patients With Stage IV Non-Small Cell Lung Cancer

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
This phase II trial tests whether CD105/Yb-1/SOX2/CDH3/MDM2-polyepitope plasmid DNA vaccine (STEMVAC) works to shrink tumors in patients with stage IV non-small cell lung cancer. STEMVAC targets specific immunogenic proteins that help lung cancer cells to grow. STEMVAC is made up of deoxyribonucleic acid (DNA), which is a natural substance in every living organism. DNA acts like a blueprint that tells all the cells in your body how to function. The DNA used in this study contains instructions for your body to produce parts of the 5 proteins the investigators identified (CDH3, CD105, YB-1, MDM2 and SOX2). STEMVAC is given with granulocyte-macrophage colony stimulating factor (GM-CSF) which is being used as an adjuvant to help create a stronger immune response. Giving STEMVAC with GM-CSF to patients while on maintenance therapy for non-small cell lung cancer (NSCLC) may help activate certain immune cells to recognize and kill lung cancer cells.
Protocol Amendment History 4 changes
critical Enrollment reopened 2026-07-28
notable Enrollment increased: 5 -> 40 participants 2026-07-28
notable Primary completion pushed: 2024-08-13 -> 2027-11-21 2026-07-28
minor Completion pushed: 2026-12-31 -> 2032-11-21 2026-07-28
Trial Details
NCT Number NCT05242965
Lead Sponsor University of Washington
Collaborators: United States Department of Defense
Conditions Lung Non-Small Cell Carcinoma, Stage IV Lung Cancer AJCC v8
Enrollment 40 participants
Start Date 2023-03-24
Primary Completion 2027-11-21 (estimated)
Study Completion 2032-11-21 (estimated)
Updated on ClinicalTrials.gov 2026-07-27