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18F-rhPSMA-7.3 PET/MRI for Prostate Cancer Active Surveillance

Phase < 1
Recruiting
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, average 1 year
Awards & highlights

Study Summary

This trial studies how PET/MRI with an imaging drug and MRI contrast can help diagnose prostate cancer in those eligible for active surveillance. Not a treatment trial.

Who is the study for?
This trial is for men with low risk or favorable intermediate risk prostate cancer confirmed by biopsy, who are following an active surveillance protocol that includes MRI and a confirmatory biopsy. It's not suitable for those without histological confirmation of prostate cancer, previous treatments for it, inability to undergo MRI due to claustrophobia or incompatible devices, or if they don't meet the criteria for active surveillance.Check my eligibility
What is being tested?
The study is testing the effectiveness of a new imaging technique using PET/MRI scans combined with an investigational radioactive drug called 18F-rhPSMA-7.3 and MRI contrast agents. This research aims to improve how doctors monitor prostate cancer in patients who are under active surveillance.See study design
What are the potential side effects?
Since this study focuses on imaging rather than treatment, side effects may be related to the PET/MRI procedure or the investigational drug used during scanning. These could include allergic reactions to contrast agents, discomfort from lying still during imaging, and exposure to radiation.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, average 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, average 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of lesions detected in total on the participants' mpMRI exams.
Secondary outcome measures
Number of lesions detected on the participants' 18F-rhPSMA-7.3 exams.
Other outcome measures
Number of malignant lesions identified on PET/MRI-guided targeted biopsy
Number of malignant lesions identified on mpMRI-guided targeted biopsy

Trial Design

1Treatment groups
Experimental Treatment
Group I: Prostate CancerExperimental Treatment1 Intervention
18F-rhPSMA-7.3 PET/MRI in Prostate Cancer Active Surveillance: A Pilot Study

Find a Location

Who is running the clinical trial?

University of Alabama at BirminghamLead Sponsor
1,590 Previous Clinical Trials
2,281,432 Total Patients Enrolled
10 Trials studying Prostate Cancer
2,717 Patients Enrolled for Prostate Cancer

Media Library

Prostate Cancer Clinical Trial Eligibility Overview. Trial Name: NCT05707182 — Phase < 1
Prostate Cancer Research Study Groups: Prostate Cancer
Prostate Cancer Clinical Trial 2023: Prostate Cancer Highlights & Side Effects. Trial Name: NCT05707182 — Phase < 1
Prostate Cancer 2023 Treatment Timeline for Medical Study. Trial Name: NCT05707182 — Phase < 1

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals under 30 years of age being included in the current research study?

"This trial has an age range of 18-89, and is thus available to adult patients."

Answered by AI

Is it still possible to submit an application for this research study?

"According to the information provided on clinicaltrials.gov, recruiting for this medical trial has ceased. Having been first posted in March of 2023 and last updated January 21st, it is among a pool of 1,294 other trials currently searching for enrollees."

Answered by AI

Is participation in this experiment feasible for me?

"Currently, this clinical trial is searching for 30 male individuals with prostate cancer between 18 and 89 years old. The specific inclusion criteria are as follows: Men who have had a biopsy that confirms low risk or favourable intermediate risk prostate cancer, scheduled to undergo multiparametric MRI scans followed by confirmatory biopsies in accordance with institutional active surveillance protocols."

Answered by AI
~20 spots leftby Dec 2026