Overview

Positron Emission Tomography Imaging Using Copper Cu 64 TP3805 in Patients With Breast Cancer

Status:
Terminated
Trial end date:
2012-07-01
Target enrollment:
0
Participant gender:
Female
Summary
This clinical trial studies positron emission tomography imaging in using copper Cu 64 TP3805in patients with breast cancer. Diagnostic procedures, such as positron emission tomography (PET) and positron emission mammography (PEM) scan, using Cu-64-TP3805 may help doctors find and diagnose breast cancer.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sidney Kimmel Cancer Center at Thomas Jefferson University
Collaborator:
National Institutes of Health (NIH)
Treatments:
Copper
Deoxyglucose
Fluorodeoxyglucose F18
Criteria
Inclusion Criteria:

- Female

- Breast cancer shown with abnormal mammogram and histology verification (stage-1
patients will also need to have a positive F-18-FDG whole-body scan)

- Tumor mass of 1 cm or larger, as determined by mammography, ultrasound, or magnetic
resonance imaging (MRI)

- Signed informed consent form approved by the institutional review board (IRB)

Exclusion Criteria:

- Pregnant or lactating female

- Patient with asthma