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

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

September 10, 2021

Primary Completion Date

June 16, 2023

Study Completion Date

September 1, 2026

Conditions
Breast Cancer
Interventions
BIOLOGICAL

DPX-Survivac

"DPX is a novel formulation that when combined with target antigens acts to activate T cells. It is a lipid-based formulation that creates a long lasting depot at the site of injection, forcing an active uptake by antigen presenting cells (APCs). APCs traffic to regional lymph nodes where naïve T cells are activated, inducing strong and sustained immune responses. All arms will receive DPX-Survivac on weeks 2 and 5."

DRUG

Letrozole 2.5mg

Aromatase inhibitor all arms will receive

DRUG

Cyclophosphamide 50mg

oral chemotherapy used in the neoadjuvant setting for Arm C only

RADIATION

XRT 10Gy x2

Directed radiation at week 4 for Arm B only

Trial Locations (1)

97213

Providence Portland Medical Center, Portland

All Listed Sponsors
lead

Providence Health & Services

OTHER