A Dose Finding Phase 1 of Sarilumab Plus Capecitabine in HER2/Neu-Negative Metastatic Breast Cancer and a Single-arm, Historically-controlled Phase 2 Study of Sarilumab Plus Capecitabine in Stage I-III Triple Negative Breast Cancer With High-Risk Residual Disease (EMPOWER)

This study looks to advance a novel and potent strategy to eliminate minimal residual disease (MRD) in triple negative breast cancer (TNBC) present even after multimodal treatment, thereby improving survival and increasing cure rate in this aggressive cancer. Patients with locally advanced TNBC are at high risk of developing lethal metastatic disease within 2 years of diagnosis, especially for those without a pathologic complete response (pCR) after neoadjuvant chemotherapy. The high risk occurs despite surgical excision of the primary tumor and axillary lymph nodes to eliminate residual disea

Trial Details

NCT ID
NCT04333706
Phase
PHASE1 / PHASE2
Sponsor
University of Southern California
Status
RECRUITING
Cancer Type
Triple Negative (TNBC) Breast Cancer
Interventions
  • Capecitabine
  • Sarilumab 150mg or 200 mg plus Capecitabine
  • Sarilumab 150mg plus Capecitabine
Locations (sample)
  • Los Angeles, California, United States|34.05223,-118.24368
  • Los Angeles, California, United States|34.05223,-118.24368
  • Gainesville, Florida, United States|29.65163,-82.32483

Key Eligibility Criteria

  • A. Written informed consent obtained from the subject and the ability for the subject to comply with all the study-related procedures.
  • B. Both males and females ≥ eighteen years of age
  • C. A clinical diagnosis of metastatic triple negative or hormone resistant, Her2/neu-negative breast cancer that has been confirmed histologically …
  • D. A life expectancy of at least 6 months. (Phase I only)

For full eligibility, visit ClinicalTrials.gov.

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