drugset / Trial / NCT02154529

Study of the Combination of KD019 and Trastuzumab in Subjects With HER2-Positive Metastatic Breast Cancer

NCT02154529

Phase 1/2 Terminated 17 enrolled Kadmon Corporation, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Evaluate the safety and tolerability and determine the maximum tolerated dose (MTD) of the combination of tesevatinib and trastuzumab in subjects with HER2-positive metastatic breast cancer

Timeline

Start
2014-05
Primary completion
2015-09-13
Completion
2015-09-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Tesevatinib Small molecule 150 mg Oral
Subject Tesevatinib Small molecule 250 mg Oral
Subject Tesevatinib Small molecule 300 mg Oral
Subject Tesevatinib Small molecule 350 mg Oral
Subject Trastuzumab Monoclonal antibody 6 mg/kg Intravenous