Overview

Phase II Study of Tetrathiomolybdate (TM) in Patients With Breast Cancer

Status:
Active, not recruiting
Trial end date:
2022-06-01
Target enrollment:
Participant gender:
Summary
Patients with moderate to high risk primary breast cancer (Stage II with more than 4 lymph nodes involved with cancer) III or Stage IV (without evidence of disease) will take tetrathiomolybdate (TM) pills for two years. The objectives of the study are to: - Assess the safety and tolerability of tetrathiomolybdate in patients with breast cancer at high risk of tumor recurrence. - Observe the disease-free survival of patients in this trial. - Conduct background scientific experiments on tumor tissue and blood of patients in this study
Phase:
Phase 2
Details
Lead Sponsor:
Memorial Sloan Kettering Cancer Center
Weill Medical College of Cornell University
Collaborator:
Weill Medical College of Cornell University
Treatments:
Molybdenum
Tetrathiomolybdate