drugset / Trial / NCT00669747

Study Of Intraductal Carboplatin In Women With Ductal Carcinoma In Situ (DCIS)

NCT00669747 ↗

Phase 2 Unknown 45 enrolled Windy Hill Medical, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to compare the safety of 100 mg carboplatin administered intraductally once on Day 1 or twice on Days 1 and 15 in women with ductal carcinoma in situ (DCIS) undergoing surgical management 2 to 4 weeks following the Day 15 intraductal infusion. Secondary objectives are to characterize the biologic and clinical effects with respect to: pharmacokinetics, extent of disease on MRI and mammogram, histopathological assessment of DCIS, and biomarker measurement of Ki-67, TUNEL and G-actin.

Timeline

Start
2008-05
Primary completion
2009-09
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 100 mg Other