Biodistribution and Safety of the PET Probes [18F]FPRGD2 and [18F]FPPRGD2



Status:Suspended
Conditions:Breast Cancer, Lung Cancer, Cancer, Cancer, Brain Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:10/14/2017
Start Date:October 2010
End Date:December 2015

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The purpose of the study is to conduct a pilot test of a new tracer in healthy human
volunteers to define normal tracer biodistribution (where the tracer goes), stability (how
much metabolises), pharmacokinetics (how much stays in which organs and for how long), and
radiation dosimetry (organ radiation dose). The same radiopharmaceutical will then be tested
in cancer patients.


Inclusion Criteria:

Healthy volunteers:

1. Must be 18 years of age or older.

2. Must have no known medical problems and have had a full medical exam within 6 months
of the study.

3. Must understand and voluntarily have signed an Informed Consent after its contents
have been fully explained.

4. Women of child bearing potential (as defined as women who are not post menopausal for
12 months or who have had no previous surgical sterilization) and men must agree to
use adequate contraception (hormonal or barrier method of birth control; abstinence)
prior to study entry, for the duration of study participation and for 30 days after
the last dose.

Cancer subjects:

1. Greater than 18 years-old at the time of radiotracer administration

2. Provides written informed consent

3. Diagnosed with advanced NSCLC, breast cancer, pancreatic cancer and GBM; patients will
undergo bevacizumab or Cyberknife therapy

4. Able to remain still for duration of each imaging procedure (about one hour)

Exclusion Criteria

1. Less than 18 years-old at the time of radiotracer administration

2. Pregnant or nursing
We found this trial at
1
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291 Campus Dr
Stanford, California 94305
(650) 725-3900
Stanford University School of Medicine Vast in both its physical scale and its impact on...
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Stanford, CA
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