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Clinical Trial Summary

The phase Ib part of the trial will assess the MTD of AUY922 in combination with Trastuzumab in patients with Trastuzumab-refractory locally advanced or metastatic HER2+. The MTD is defined as the highest drug dosage not causing in the first cycle of treatment (28 days) medically unacceptable dose limiting toxicity (DLT). The phase II part of the trial will assess any potential effect on efficacy of adding AUY922 to Trastuzumab in patients with Trastuzumab-refractory locally advanced or metastatic HER2+ breast cancer. Both AUY922 and Trastuzumab will be administered as a weekly IV infusion. Treatment should be continued as long as the patient does not have disease progression and tolerates the treatment. The following reasons are examples of acceptable reasons for discontinuing the study; tumor progression (by RECIST, as assessed by the investigator), unacceptable toxicity, death, or discontinuation from the study for any other reason, such as patient refusal, withdrawn consent, lost to follow-up or investigator decision.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01271920
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 1/Phase 2
Start date September 2010
Completion date October 2013

See also
  Status Clinical Trial Phase
Completed NCT01921335 - ARRY-380 + Trastuzuamab for Breast w/ Brain Mets Phase 1