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Clinical Trials/NCT02079181
NCT02079181
Terminated
Not Applicable

18F-FMAU for Imaging in Cancer Patients

University of Southern California1 site in 1 country3 target enrollmentJanuary 31, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malignant Neoplasm
Sponsor
University of Southern California
Enrollment
3
Locations
1
Primary Endpoint
Radiation dosimetry of fluorine F 18 d-FMAU
Status
Terminated
Last Updated
last year

Overview

Brief Summary

This clinical trial studies the safety and drug distribution of the radioactive drug, 2'-deoxy-2'-[18F]fluoro-5-methyl-1-beta-D-arabinofuranosyluracil (fluorine F 18 d-FMAU [18F-FMAU]), for imaging with positron emission tomography/computed tomography (PET/CT) in patients with advanced cancers. A PET scan is a procedure in which a small amount of radioactive glucose (sugar) is injected into a vein, and a scanner is used to make detailed, computerized pictures of areas inside the body where the glucose is taken up. Because cancer cells often take up more glucose than normal cells, the pictures can be used to find cancer cells in the body. PET/CT using the drug fluorine F 18 d-FMAU, may help find cancer and find out how far the disease has spread.

Detailed Description

PRIMARY OBJECTIVES: I. To determine the radiation dosimetry of 18F-FMAU in humans, confirm absence of adverse events in humans from intravenous (i.v.) injection of 18F-FMAU for PET imaging, and characterize the incidence of circulating metabolites of 18F-FMAU in humans. II. To simply find out whether there is any visual uptake change of 18F-FMAU in tumors post-therapy. OUTLINE: Patients receive fluorine F 18 d-FMAU IV followed by PET/CT prior to start of cancer treatment. Patients may undergo 2 additional scans at one week prior to second course of chemotherapy and after completion of cancer treatment depending on cancer type.

Registry
clinicaltrials.gov
Start Date
January 31, 2014
End Date
August 22, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Have been diagnosed with a malignancy/tumor/cancer, including but not limited to: brain tumor, breast cancer, lung cancer, esophageal cancer, lymphoma, or sarcoma
  • Have one or more tumors visualized by conventional PET-CT, CT or magnetic resonance imaging (MRI) prior to the PET FMAU study; PET-CT should be within one week prior to 18F-FMAU

Exclusion Criteria

  • Have undergone chemotherapy or radiation therapy within the previous one month
  • Women of childbearing potential, unless they have had a negative urine beta human chorionic gonadotropin (betaHCG) within the previous 24 hours of the procedure
  • Patients who have had surgery at the site of the suspected lesion within 1 month

Outcomes

Primary Outcomes

Radiation dosimetry of fluorine F 18 d-FMAU

Time Frame: Up to 24 hours after fluorine F 18 d-FMAU PET/CT scan

Adverse events after injection of fluorine F 18 d-FMAU to the patients

Time Frame: Up to 24 hours after fluorine F 18 d-FMAU PET/CT scan

Fluorine F 18 d-FMAU uptake change in tumors post-therapy

Time Frame: Baseline up to 24 hours after fluorine F 18 d-FMAU PET/CT scan

Study Sites (1)

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