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COMPLETED
NCT04510311
EARLY_PHASE1

Imaging Properties of PET Radiotracer [18F]3F-PHPG in Patients With Neuroendocrine Tumors

Sponsor: University of Michigan Rogel Cancer Center

View on ClinicalTrials.gov

Summary

The goal of this exploratory study is to test whether \[18F\]3F-PHPG can be used reliably to map the locations of tumors in patients with neuroendocrine tumors. If so, the results of this study will be used to support further development of \[18F\]3F-PHPG as a clinical tool for neuroendocrine tumor localization and staging.

Official title: An Exploratory Study of 3-[18F]Fluoro-para-hydroxyphenethylguanidine ([18F]3F-PHPG) in Patients With Neuroendocrine Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2020-10-19

Completion Date

2024-12-31

Last Updated

2026-06-08

Healthy Volunteers

No

Interventions

DRUG

3-[18F]Fluoro-para-hydroxyphenethylguanidine

Single IV injection of 12.0 mCi (+/- 10%) \[18F\]3F-PHPG

DRUG

[123I] metaiodobenzylguanidine

Single IV injection of 10.0 mCi \[123I\]MIBG

DIAGNOSTIC_TEST

Positron emission tomography/computed tomography scan

Whole-body PET/CT scan performed at two time-points: 1.5 hours and 3 hours after IV injection of \[18F\]3F-PHPG

DIAGNOSTIC_TEST

Planar scintigraphy scan

Whole-body scan using planar scintigraphy with a gamma camera performed the day after IV injection of \[123I\]MIBG

DIAGNOSTIC_TEST

Single photon emission computed tomography/computed tomography scan

SPECT/CT scan of the primary neuroendocrine tumor performed the day after IV injection of \[123I\]MIBG

Locations (1)

University of Michigan Rogel Cancer Center

Ann Arbor, Michigan, United States