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Diagnostic Test
PSMA-PET + MRI for Prostate Cancer
Phase 2 & 3
Recruiting
Led By Clinton Bahler, MD
Research Sponsored by Five Eleven Pharma, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Significant prostate cancer: Gleason 3+4 ≥1 core with pattern 4 ≥20% OR ≥3 cores of Gleason 3+4 OR Any Gleason 4+3, 4+4, 4+5, 5+4, or 5+5
Men diagnosed with prostate cancer who choose radical prostatectomy
Must not have
Patient is unable to tolerate remaining still on the bed of the PET or MRI camera, due to physical limitations or claustrophobia
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is comparing two groups of patients undergoing surgery. One group will receive the usual imaging scan, while the other group will get an additional special scan that uses a dye to make cancer cells more visible. This new imaging method may help doctors plan surgeries better and improve patient outcomes.
Who is the study for?
Men with significant prostate cancer planning to undergo surgery can join. They should have a certain level of prostate cancer severity, based on Gleason scores, and wish to maintain erections post-treatment. Men with any serious health issues, participating in other radiation trials recently, or unable to stay still for imaging due to physical limits or claustrophobia cannot participate.
What is being tested?
The trial is testing if adding a PSMA-PET scan alongside the standard MRI before surgery provides better information than just the MRI alone. The study will see if this extra scan changes surgical plans and improves outcomes by comparing two groups: one gets only an MRI and the other gets both an MRI and PSMA-PET.
What are the potential side effects?
Since this trial involves diagnostic procedures rather than medications, side effects are minimal but may include discomfort from lying still during scans and potential anxiety related to claustrophobia in imaging devices.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My prostate cancer is aggressive based on my biopsy results.
Select...
I am a man with prostate cancer opting for surgery to remove my prostate.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot stay still on a PET or MRI machine due to physical issues or claustrophobia.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 18 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
IIEF-EF sub scale score
Secondary study objectives
Therapeutic procedure
EPE detection
Erectile dysfunction: ability to achieve erection sufficient for penetration
+5 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: PSMA-PET and SOC MRI prior to surgeryExperimental Treatment1 Intervention
Group II: SOC MRI prior to surgeryActive Control1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Prostate cancer treatments often involve advanced imaging techniques like the PSMA PET scan, which uses a radiotracer that binds to the Prostate-Specific Membrane Antigen (PSMA) on prostate cells. This allows for highly precise imaging, aiding in the detection of micrometastatic disease and guiding treatment decisions.
Other treatments include hormone therapy, which reduces androgen levels to slow cancer growth, and radiotherapy, which uses high-energy radiation to kill cancer cells. These mechanisms are crucial as they enable personalized treatment plans, improve detection of disease spread, and potentially enhance patient outcomes by targeting cancer more effectively.
Effect of <sup>18</sup>F-DCFPyL PET/CT on the Management of Patients with Recurrent Prostate Cancer: Results of a Prospective Multicenter Registry Trial.Incorporating PSMA-Targeting Theranostics Into Personalized Prostate Cancer Treatment: a Multidisciplinary Perspective.Current Use of Imaging after Primary Treatment of Prostate Cancer.
Effect of <sup>18</sup>F-DCFPyL PET/CT on the Management of Patients with Recurrent Prostate Cancer: Results of a Prospective Multicenter Registry Trial.Incorporating PSMA-Targeting Theranostics Into Personalized Prostate Cancer Treatment: a Multidisciplinary Perspective.Current Use of Imaging after Primary Treatment of Prostate Cancer.
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Who is running the clinical trial?
Five Eleven Pharma, Inc.Lead Sponsor
5 Previous Clinical Trials
122 Total Patients Enrolled
3 Trials studying Prostate Cancer
104 Patients Enrolled for Prostate Cancer
Indiana UniversityOTHER
1,037 Previous Clinical Trials
1,218,685 Total Patients Enrolled
8 Trials studying Prostate Cancer
365 Patients Enrolled for Prostate Cancer
Clinton Bahler, MDPrincipal InvestigatorIndiana University School of Medicine
2 Previous Clinical Trials
51 Total Patients Enrolled
2 Trials studying Prostate Cancer
51 Patients Enrolled for Prostate Cancer
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I want to keep my ability to have erections after treatment.I cannot stay still on a PET or MRI machine due to physical issues or claustrophobia.My prostate cancer is aggressive based on my biopsy results.I do not have any major health issues that could interfere with the study.I am a man with prostate cancer opting for surgery to remove my prostate.
Research Study Groups:
This trial has the following groups:- Group 1: PSMA-PET and SOC MRI prior to surgery
- Group 2: SOC MRI prior to surgery
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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