Suspended

A Phase I/II Imaging Study of 1-a-D-(5-deoxy-5-[18]F-fluoroarabinofuranosyl)-2-nitroimidazole ([18]F-FAZA) in Patients With Known Squamous Cell Carcinoma of the Head & Neck, Small Cell and Non-Small Cell Carcinoma of the Lung, Lymphoma, Glioblastoma Multiforme, Neuroendocrine Tumours or Renal Cell Carcinoma

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What is being tested

18F-FAZA PET Imaging

Drug
Who is being recruted

Urogenital Diseases+17

+ Adenocarcinoma

+ Carcinoma

Over 16 Years
+3 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Phase 1 & 2
Interventional
Study Start: September 2006
See protocol details

Summary

Principal SponsorAHS Cancer Control Alberta
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 12, 2006

Actual date on which the first participant was enrolled.

This is a diagnostic study that focuses on a specific type of imaging called 18F-FAZA PET scan. The study involves patients who have been diagnosed with certain types of cancer, including squamous cell carcinoma of the Head & Neck, small cell and non-small cell carcinoma of the lung, lymphoma, glioblastoma multiforme, neuroendocrine tumors, or renal cell carcinoma. The main goal of this study is to ensure the safety of 18F-FAZA, a substance used in the imaging process, and to understand how it spreads within the body. This research is important as it could potentially improve the way these cancers are diagnosed and treated. The study consists of two phases. In the first phase, patients will undergo a single 18F-FAZA PET scan. Their vital signs, blood test results, and any adverse events will be carefully monitored before the injection and after the imaging. In the second phase, patients will receive three 18F-FAZA PET scans: one before treatment, one during the middle of the treatment, and one after the treatment. The study will examine where the 18F-FAZA goes in the body and how much is taken up by normal and abnormal tissues.

Official TitleA Phase I/II Imaging Study of 1-a-D-(5-deoxy-5-[18]F-fluoroarabinofuranosyl)-2-nitroimidazole ([18]F-FAZA) in Patients With Known Squamous Cell Carcinoma of the Head & Neck, Small Cell and Non-Small Cell Carcinoma of the Lung, Lymphoma, Glioblastoma Multiforme, Neuroendocrine Tumours or Renal Cell Carcinoma
NCT00323076
Principal SponsorAHS Cancer Control Alberta
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

92 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 16 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesAdenocarcinomaCarcinomaCarcinoma, Renal CellFemale Urogenital Diseases and Pregnancy ComplicationsKidney DiseasesKidney NeoplasmsNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Germ Cell and EmbryonalNeoplasms, Glandular and EpithelialNeoplasms, Nerve TissueUrogenital NeoplasmsUrologic DiseasesUrologic NeoplasmsNeuroectodermal TumorsNeuroendocrine TumorsFemale Urogenital DiseasesMale Urogenital Diseases

Criteria

3 inclusion criteria required to participate
Male or female greater than or equal to 16 years of age.

If female of child-bearing potential and outside of the window of 10 days since the first day of the last menstrual period, a negative pregnancy test is required.

Patients with known primary or suspected metastatic squamous cell carcinoma of the head and neck, non-small cell or small cell carcinoma of the lung, lymphoma, GBM (greater than or equal to 3 glioma), neuroendocrine tumours, or renal cell carcinoma with at least one lesion >1 cm in diameter.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
18F-FAZA PET Imaging

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Cross Cancer Institute

Edmonton, CanadaOpen Cross Cancer Institute in Google Maps
SuspendedOne Study Center