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RecruitingNCT06462495Updated Jun 17, 2024

Head-to-head Comparison of [18F]F-PSMA-N5 With [18F]F-PSMA-1007 PET/CT in PCa Diagnosis, Recurrence, and Metastasis

An Early Phase 1 interventional study of [18F]F-PSMA-N5 and [18F]F-PSMA-1007 in Prostate Cancer and PET/CT, sponsored by Anhui Provincial Hospital. Recruiting at 1 site in China. Open to male participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-17.

Sponsored by Anhui Provincial Hospital · Early Phase 1, Interventional, and Diagnostic

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as recruiting.
  • Started Apr 2024; still recruiting 2 years 5 months later.
Phase
Early Phase 1
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years to 90 Years
Sex
Male
01

Study summary

To prospectively evaluate the radiodrug biodistribution of a novel PET imaging agent [18F]F-PSMA-N5 in different organs of prostate cancer patients and its diagnostic efficacy in the diagnosis, recurrence and metastasis of prostate cancer, and to compare with [18F]F-PSMA-1007.

Read the detailed description

[18F]F-PSMA-N5 PET/CT was used for initial assessment of prostate cancer or detection of recurrence. The maximum standardized uptake value (SUVmax) was used to evaluate tumor uptake. The sensitivity, specificity, the number and accuracy of lesions identified and the distribution of lesions in each organ were calculated and compared with those of [18F]F-PSMA-1007 PET/CT.

02

Conditions studied

  • Prostate Cancer
  • PET/CT
03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,399 are open to participants now.

This study's planned enrollment of 30 is below the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Anhui Provincial Hospital is the lead sponsor of 129 studies on the registry; 95 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged from 18 to 90 years old;
  • Complete MRI images and clinical data (such as PSA level, Gleason grade, etc.);
  • Prostate cancer detected by PSA or imaging examination, or clinically suspected recurrence after standardized treatment;
  • simultaneous [18F]F-PSMA-N5 and [18F]F-PSMA-1007 examinations within two weeks;
  • Willing to undergo surgery or needle biopsy for pathological examination after examination, or confirmed as prostate cancer by histopathology before or after treatment;
  • Sign informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patients who cannot cooperate with the examination;
  • Concurrent malignant tumors;
  • Previous alcohol allergy;
  • Patients with liver and kidney dysfunction;
  • Other circumstances deemed by the investigator to be inappropriate for trial participation.
05

Study design

Phase
Early Phase 1
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    [18F]F-PSMA-N5 and [18F]F-PSMA-1007 PET/ CT scan

    Subjects PET/CT imaging: On any two days for two consecutive weeks, each subject underwent a PET/ CT scan after intravenous injection of \[18F\]F-PSMA-N5 and \[18F\]F-PSMA-1007.

    Drug: [18F]F-PSMA-N5 · Drug: [18F]F-PSMA-1007

Interventions

  • Drug[18F]F-PSMA-N5

    Each subject receive a single intravenous injection of \[18F\]F-PSMA-N5, and undergo PET/CT imaging within the specificed time.

    Also known as: [18F]F-PSMA-N5 injection

  • Drug[18F]F-PSMA-1007

    Each subject receive a single intravenous injection of \[18F\]F-PSMA-1007, and undergo PET/CT imaging within the specificed time.

    Also known as: [18F]F-PSMA-1007 injection

06

What researchers measure

Primary outcomes

  1. Standard uptake value(SUV)

    Standard uptake value(SUV) of \[18F\]F-PSMA-N5 and \[18F\]F-PSMA-1007 for each target lesion of subjects.

    Time frame: 30 days

Secondary outcomes

  1. Diagnostic efficacy

    The sensitivity, specificity and accuracy of \[18F\]F-PSMA-N5 and \[18F\]F-PSMA-1007 PET/CT were calculated.

    Time frame: 30 days

  2. Number of lesions

    The number of lesions detected by \[18F\]F-PSMA-N5 and \[18F\]F-PSMA-1007 PET/CT.

    Time frame: 30 days

07

Study locations

1 of 1 sites recruiting
  • The First Affiliated Hospital of China University of Science and Technology(Anhui Provincial Hospital)
    Hefei, Anhui 230000, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06462495
Lead sponsor
Anhui Provincial Hospital
Responsible party
Sponsor
First posted
Jun 17, 2024
Start date
Apr 10, 2024
Primary completion
Jun 30, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jun 17, 2024

Study contacts

Qiang Xie, MD
Contact
xieqiang1980@ustc.edu.cn
+8613721108043
Qiang Xie
study chair · The First Affiliated Hospital of USTC (Anhui Provincial Hospital)

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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