68Ga-P3 PET/CT Imaging in Prostate
A Study to Evaluate 68Ga-P3 PET/CT Imaging of PSMA Expression in Prostate
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 29, 2023
CompletedFirst Submitted
Initial submission to the registry
July 4, 2023
CompletedFirst Posted
Study publicly available on registry
July 11, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2025
CompletedNovember 7, 2024
October 1, 2024
2.2 years
July 4, 2023
November 5, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
The diagnostic efficacy of 68Ga-P3 PET/CT in the evaluation of Prostate
the standardized Uptake Value (SUV) of lesions on 68Ga-P3 PET/CT
1 year
The detection efficacy of 68Ga-P3 PET/CT in the evaluation of Prostate
the number of lesions detected by 68Ga-P3 PET/CT, based on the pathology or clinical follow-up as gold standard.
1 year
Secondary Outcomes (3)
The dosimetry of 68Ga-P3
1 year
Quantitative evaluation of 68Ga-P3
1 year
Correlation with pathological expression
1 year
Study Arms (1)
[68Ga]P3
EXPERIMENTALSubjects with suspected or confirmed Prostate will receive an intravenous injection of 68Ga-P3 followed by PET imaging.
Interventions
68Ga-P3 is injected intravenously with a dose of 0.06-0.08 mCi/kg.
Eligibility Criteria
You may qualify if:
- patients with confirmed or suspected cancer; Signed written informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University First Hospital
Beijing, Beijing Municipality, 100034, China
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 4, 2023
First Posted
July 11, 2023
Study Start
May 29, 2023
Primary Completion
July 31, 2025
Study Completion
July 31, 2025
Last Updated
November 7, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share