Cancer Clinical Trial - 68-Ga-FAPI PET Imaging in Malignancy

Status Not yet recruiting

Clinical Trial Summary

This feasibility trial studies the use of gallium-68 (68Ga)-FAPI as the imaging agent for positron emission tomography (PET)/computed tomography (CT), collectively PET/CT, in patients with various cancers. PET uses a radioactive substance called 68Ga-FAPI, which attaches to cancer activated fibroblasts. The PET scanner takes pictures that capture where the radioactive drug is "lighting up" and attaching to tumor cells, which may help doctors recognize differences between tumor and healthy tissue. CT uses X-rays to make a picture of areas inside the body. Using 68Ga-FAPI in diagnostic procedures, such as PET/CT, may allow doctors to identify smaller tumors than standard imaging.

Clinical Trial Description

PRIMARY OBJECTIVE: To assess feasibility and biodistribution of PET imaging in malignancy using 68Ga-FAPI. OUTLINE: Patients receive 68Ga-FAPI intravenously (IV) and then undergo PET/CT approximately 1 hour later. After completion of study, patients are followed up at 24-72 hours. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04023240
Study type	Interventional
Source	Stanford University
Contact	Risa Jiron
Phone	650-736-1598
Email	rjiron@stanford.edu
Status	Not yet recruiting
Phase	Phase 2
Start date	July 2023
Completion date	December 14, 2023

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