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NCT05160480

A Pilot Study of Total-body PET Using FDA-approved Radiotracers Beyond 18F-FDG

ENROLLING BY INVITATION Last updated 10 March 2026
What this trial tests

trial testing Total-body PET imaging in Prostate Cancer in 9 participants. Enrolling by invitation.

Timeline
7 June 2024
Primary endpoint
1 September 2026
1 September 2026

Quick facts

Lead sponsorUniversity of California, Davis
StatusENROLLING BY INVITATION
Study typeOBSERVATIONAL
Enrollment9
Start date7 June 2024
Primary completion1 September 2026
Estimated completion1 September 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, Davis

Who can join

18 and older, any sex, with Prostate Cancer or Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research study is to test new ways to improve the usefulness of the world's first total-body positron emission tomography (PET)/computed tomography (CT) scanner (EXPLORER) by collecting data from PET scans using one of three different imaging agents: 18F-PSMA; 18F-FES; or, 68Ga DOTATATE. These imaging agents are approved by the FDA to be used for patients diagnosed with prostate cancer (18F-PSMA), neuroendocrine tumor (68Ga DOTATATE), or breast cancer (18F-FES).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Prostate Cancer

Currently open trials in the same condition.

Other University of California, Davis trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05160480.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing