Skip to content

A Radiopharmacokinetic and Radiodosimetric Phase I Imaging Study of 18F-FAZA

A Radiopharmacokinetic and Radiodosimetric Phase I Imaging Study of 18F-FAZA

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00756691
Enrollment
0
Registered
2008-09-22
Start date
Unknown
Completion date
Unknown
Last updated
2017-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxic Tumours

Keywords

18F-FAZA, Positron Emission Tomography, Radiation dosimetry, Pharmacokinetics

Brief summary

Hypoxia (little of no oxygen) is considered to be an important characteristic of a patient's tumour that may help predict patient outcomes and/or help inform patient management decisions. 18F-FAZA Positron Emission Tomography (PET) can detect hypoxic tumours because 18F-FAZA accumulates in hypoxic tissues. This study is being done to learn more about the processes by which 18F-FAZA is absorbed, distributed, metabolized (built-up and broken down) and eliminated by the body.

Detailed description

A Phase I Radiopharmacokinetic and Radiodosimetric study of 18F-FAZA. Prior to treatment, subjects will receive a single injection of 18F-FAZA. Subjects will undergo a series of 5-5 PET scans, and will have 8-13 blood samples and 2 urine samples taken at specified time points over a 4.5-5.5 hour period. 18F-FAZA PET images will be reviewed to develop a dynamic uptake model, and blood and urine samples will be analyzed for unchanged 18F-FAZA and its metabolites.

Interventions

Radioactive dose of 110-600 MBq per injection. A single pre-treatment injection of 18F-FAZA will be permitted per patient

Sponsors

AHS Cancer Control Alberta
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male of Female \> or = to 18 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 required * Subjects with known primary or suspected metastatic SCC head and neck; NSCLC; SCLC; GBM; lymphoma, or NET with at least one lesion \> 1 cm in diameter * Able and willing to follow instructions and comply with the protocol * Provide written informed consent prior to participation in the study * Karnofsky Performance Scale Score of 70-100

Exclusion criteria

* Previous treatment for their primary or metastatic SCC head and neck, NSCLC, SCLC, GBM, Lymphoma, or NET * Bilirubin \> or = to 200 umol/L * Creatinine \> or - to 150 umol/L * AST or ALT \> or = to 5 times the upper limits of normal * Serious medical conditions such as: congestive heart failure, unstable angina, unstable ventricular arrhythmia, uncontrolled psychiatric conditions, serious infections, uncontrolled diabetes * Nursing or pregnant females

Design outcomes

Primary

MeasureTime frame
To Collect imaging-based data for radiopharmacokinetic and radiodosimetric analyses.2 years

Secondary

MeasureTime frame
To determine radiation dosimetry and optimal imaging times2 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026