MedPath

68Ga-PSFA PET Imaging in Patients With PSMA/FAP Positive Disease

Early Phase 1
Recruiting
Conditions
PSMA
FAP
Positron-Emission Tomography
Interventions
Registration Number
NCT06387381
Lead Sponsor
First Affiliated Hospital of Chongqing Medical University
Brief Summary

As a new dual receptor (PSMA and FAP) targeting PET radiotracer, 68Ga-PSFA is promising as an excellent imaging agent applicable to PSMA/FAP positive diseases. In this research, we investigate the safety, biodistribution and potential usefulness of 68Ga-PSFA positron emission tomography (PET) for the diagnosis of lesions in PSMA/FAP positive diseases.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  1. At least 18 years of age.
  2. Signed informed consent.
  3. Patients with suspected or newly diagnosed or previously malignant disease, with either PSMA or FAP positive expression (supporting evidence may include MRI, CT, and pathology report, etc).
Exclusion Criteria
  1. Patients with non-malignant disease.
  2. Patients with pregnancy.
  3. The inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.
  4. Known or expected hypersensitivity to 68Ga-PSFA or any of its components.
  5. Any serious medical condition or extenuating circumstance which the investigator feels may interfere with the procedures or evaluations of the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
68Ga-PSFA68Ga-PSFAPatients will receive a single administration of 68Ga-PSFA.
Primary Outcome Measures
NameTimeMethod
Diagnostic efficacy15 days

The sensitivity, specificity, and accuracy of 68Ga-PSFA PET

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The First Affiliated Hospital of Chongqing Medical University

🇨🇳

Chongqing, Chongqing, China

© Copyright 2025. All Rights Reserved by MedPath