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Recruiting NCT05940259

68Ga-P3 PET/CT Imaging in Prostate

No phase Interventional Neoplasms

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: [68Ga]P3.
Who it may be relevant to
Registry conditions: Neoplasms. Basic parameters: 18 years — 75 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Study to Evaluate 68Ga-P3 PET/CT Imaging of PSMA Expression in Prostate

Overview

Prostate-specific membrane antigen (PSMA) is a type II transmembrane glycoprotein that consists of 750 amino acids. It is highly expressed on most prostate cancer cells and neovascular endothelial cells of tumors, making PSMA a highly specific and significant imaging target for malignancies. \[68Ga\]P3, a novel molecular probe of PET imaging agent that targets PSMA, can be used in the diagnosis and research of a wide variety of PSMA high-expression malignanciesr.

Detailed description

Prostate-specific membrane antigen (PSMA) is a type II transmembrane glycoprotein that consists of 750 amino acids. It is highly expressed on most prostate cancer cells and neovascular endothelial cells of tumors, making PSMA a highly specific and significant imaging target for malignancies.\[68Ga\]P3, a novel molecular probe of PET imaging agent that targets PSMA, can be used in the diagnosis and research of a wide variety of PSMA high-expression malignanciesr.

Interventions

  • Drug [68Ga]P3
    68Ga-P3 is injected intravenously with a dose of 0.06-0.08 mCi/kg.

Primary outcome measures

  • The diagnostic efficacy of 68Ga-P3 PET/CT in the evaluation of Prostate [Time frame: 1 year]
  • The detection efficacy of 68Ga-P3 PET/CT in the evaluation of Prostate [Time frame: 1 year]
Secondary outcome measures (3)
  • The dosimetry of 68Ga-P3 [Time frame: 1 year]
  • Quantitative evaluation of 68Ga-P3 [Time frame: 1 year]
  • Correlation with pathological expression [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

patients with confirmed or suspected cancer; Signed written informed consent

Exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

China · 1 center
  • Peking University First Hospital — Beijing

Identifiers

NCT: NCT05940259 · [68Ga] P3

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗