drugset / Trial / NCT04895761

Neoadjuvant DPX-Survivac Aromatase Inhibition, Radiotherapy or Cyclophosphamide in HR+HER2- Breast Cancer

NCT04895761

Phase 1 Active not recruiting 6 enrolled Providence Health & Services
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The study seeks to establish the safety of neoadjuvant aromatase inhibitor with: DPX-Survivac, DPX-Survivac plus radiation, or DPX-Survivac with cyclophosphamide in stage I to III HR+HER2- breast cancer. There will be sequential enrollment into 3 arms with an anticipated N=6 participants per arm for N=18 participants in total. All participants will receive letrozole 2.5 mg daily during the 6 weeks of neoadjuvant therapy. Neoadjuvant therapy occurs weeks 1-6, with standard of care surgery taking place week 7 to 9.

Timeline

Start
2021-09-10
Primary completion
2023-06-16
Completion
2026-09-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 50 mg Oral
Subject maveropepimut-S Vaccine 0.25 ml Subcutaneous
Background Letrozole Other / unclassified 2.5 mg Oral

Indications