drugset / Trial / NCT00773344

Clinical Trial of the Combination of Trastuzumab (Herceptin) and Tanespimycin in Patients With Solid Tumors and Her2 Positive Metastatic Breast Cancer That Have Previously Failed Herceptin

NCT00773344

Phase 1/2 Completed 25 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose(s) of this study is to determine the highest tolerated dose of tanespimycin and to determine anti-tumor activity (via objective response rate) of tanespimycin in patients with breast cancer who have not previously responded to Herceptin

Timeline

Start
2005-12
Primary completion
2009-05
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject tanespimycin Unknown 225 mg/m2 Intravenous
Subject tanespimycin Unknown 300 mg/m2 Intravenous
Subject tanespimycin Unknown 375 mg/m2 Intravenous
Subject tanespimycin Unknown 400 mg/m2 Intravenous

Indications