drugset / Trial / NCT01674842

Cisplatin + RT for Triple Negative Breast Cancer

NCT01674842 ↗

Phase 1 Completed 55 enrolled Dana-Farber Cancer Institute
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I dose escalation study of cisplatin and concurrent radiation in patients with ER negative, PR negative and HER2 negative breast cancer who have undergone breast-conserving surgery or mastectomy. Primary objective: To assess the safety, tolerability, and maximum tolerated dose (MTD) of cisplatin when given concurrently with radiation therapy for participants with Stage II or III breast cancer who have undergone breast conserving surgery or mastectomy

Timeline

Start
2012-10
Primary completion
2018-08
Completion
2021-06-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 10 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 20 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 30 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 40 mg/m2 Intravenous

Indications