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Active Not RecruitingNCT05455658

STEMVAC in Patients With Early Stage Triple Negative Breast Cancer

A Phase II Trial of The Immunogenicity of a DNA Plasmid Based Vaccine (STEMVAC) Encoding Th1 Selective Epitopes From Five Antigens Associated With Breast Cancer Stem Cells (MDM2, YB1, SOX2, CDC25B, CD105) in Participants With Early Stage Triple Negative Breast Cancer

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
33 (actual)
Sponsor
University of Washington · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase II trial studies the effect of DNA plasmid based vaccine (STEMVAC) in treating patients with patients with stage IB-III triple negative breast cancer. STEMVAC may wake up the immune system in patients who have had a diagnosis of triple negative breast cancer and have been treated. STEMVAC targets proteins that are expressed on breast cancer cells and works by boosting the immune system to recognize and destroy the invader cancer cell proteins that are causing the disease. The purpose of this trial is to test the immune system's response to STEMVAC.

Detailed description

OUTLINE: Patients receive STEMVAC vaccine with sargramostim intradermally (ID) every month for 3 months in the absence of disease progression or unacceptable toxicity. Patients then receive STEMVAC vaccine with sargramostim ID booster injections 3 months after the 3rd vaccination and 6 months after the 1st booster vaccination. After completion of study treatment, patients are followed up at 28 days, and then annually for 5 years.

Conditions

Interventions

TypeNameDescription
BIOLOGICALCD105/Yb-1/SOX2/CDH3/MDM2-polyepitope Plasmid DNA VaccineGiven IV
BIOLOGICALSargramostimGiven ID

Timeline

Start date
2022-11-17
Primary completion
2026-07-16
Completion
2028-07-16
First posted
2022-07-13
Last updated
2025-10-24

Locations

3 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05455658. Inclusion in this directory is not an endorsement.