Clinical Trials Directory

Trials / Completed

CompletedNCT01816035

Trastuzumab Emtansine in Treating Patients With HER2-Positive Metastatic or Locally Advanced Breast Cancer That Cannot Be Removed by Surgery

Thrombokinetic Studies of Ado-Trastuzumab Emtansine

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
13 (actual)
Sponsor
University of Washington · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase I trial studies the side effects and best way of giving trastuzumab emtansine in treating patients with human epidermal growth factor receptor 2 (HER2)-positive breast cancer that has spread to other parts of the body or nearby tissue and cannot be removed by surgery. Biological therapies, such as trastuzumab emtansine, may stimulate the immune system in different ways and stop cancer cells from growing.

Detailed description

PRIMARY OBJECTIVES: I. To assess change in thrombokinetics (platelet circulation life span). SECONDARY OBJECTIVES: I. Benefit rate (as defined by stable disease, partial response, or complete response by Response Evaluation Criteria in Solid Tumors \[RECIST\] v 1.1) at the end of study activities. II. To evaluate the safety of trastuzumab emtansine (ado-trastuzumab emtansine) (non-platelet toxicity). III. To evaluate the pharmacokinetics of ado-trastuzumab emtansine. OUTLINE: Patients receive trastuzumab emtansine intravenously (IV) over 30-90 minutes on day 1. Treatment repeats every 21 days for 3 courses in the absence of disease progression or unacceptable toxicity. Patients achieving response may continue treatment. After completion of study treatment, patients are followed up periodically.

Conditions

Interventions

TypeNameDescription
OTHERLaboratory Biomarker AnalysisCorrelative studies
OTHERPharmacological StudyCorrelative studies
BIOLOGICALTrastuzumab EmtansineGiven IV

Timeline

Start date
2014-06-01
Primary completion
2016-12-01
Completion
2017-04-01
First posted
2013-03-21
Last updated
2017-05-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01816035. Inclusion in this directory is not an endorsement.