ProAgio in Combination With Gemcitabine in Patients With Metastatic Triple Negative Breast Cancer

This is a Phase I/II Trial Evaluating the Safety and Efficacy of ProAgio, an anti- αvβ3 Integrin Cytotoxin, in Combination with Gemcitabine in Patients with Metastatic Triple Negative Breast Cancer

Trial Details

NCT ID
NCT06460298
Phase
PHASE1 / PHASE2
Sponsor
ProDa BioTech, LLC
Status
RECRUITING
Cancer Type
Triple Negative (TNBC) Breast Cancer
Interventions
  • ProAgio Dose Levels (DL) 1,2,3,4
  • ProAgio Dose Expansion
Locations (sample)
  • Atlanta, Georgia, United States|33.749,-84.38798
  • Atlanta, Georgia, United States|33.749,-84.38798

Key Eligibility Criteria

  • Adult participants, ≥ 18 years of age, with histologically or cytologically confirmed metastatic breast cancer that is estrogen receptor (ER) negat…
  • Participants must have received at least two lines of prior systemic treatment for advanced disease. If participants received systemic therapy in t…
  • ECOG performance status ≤2
  • Participants must have adequate organ and marrow function as defined below:

For full eligibility, visit ClinicalTrials.gov.

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