NCT06813898

An Investigational Scan (rhPSMA-7.3 PET/CT) for Detecting Biochemically Recurrent Prostate Cancer, ENLIGHTEN Trial

ENLIGHTEN: Detection by POSLUMA Following Negative Other PET-PSMA Imaging

• Status: Recruiting
• Phase: EARLY_Phase 1
• Study type: Interventional
• Enrollment: 27 (estimated)
• Sponsor: Northwestern University · Academic / Other
• Sex: Male
• Age: —
• Healthy volunteers: Not accepted

Summary

This phase II trial evaluates an imaging technique (rhPSMA-7.3 positron emission tomography \[PET\]/computed tomography \[CT\]) for detecting prostate cancer in patients who have increasing prostate-specific antigen levels following prior treatment (biochemical recurrence) but who were prostate specific membrane antigen negative on their most recent PET scan. Contrast agents like rhPSMA-7.3 (also called POSLUMA) circulate in the blood until they find their intended target. Once they are taken up by the target tumor cells, they can be visualized using PET/CT cameras. A PET scan is a procedure in which a small amount of radioactive tracer (in this case rhPSMA-7.3) is injected into a vein, and a scanner is used to make detailed, computerized pictures of areas inside the body where the tracer is taken up. Because tumor cells often take up more tracer than normal cells, the pictures can be used to find tumor cells in the body. A CT scan is a procedure that uses a computer linked to an x-ray machine to make a series of detailed pictures of areas inside the body. The pictures are taken from different angles and are used to create 3-dimensional views of tissues and organs. Combining a PET scan with a CT scan can help make the image easier to interpret. PET/CT scans are hybrid scanners that combine both modalities into a single scan during the same examination. The researchers want to determine whether the rhPSMA7.3 PET/CT scan is useful for detecting biochemically recurrent prostate cancer in patients who were negative on prior non-POSLUMA PET imaging.

Detailed description

PRIMARY OBJECTIVE: I. Determine consensus detection rate by flotufolastat F-18 gallium (rhPSMA-7.3)-PET (POSLUMA) scan in men with recent negative non-POSLUMA PET prostate specific membrane antigen (PSMA) scans. SECONDARY OBJECTIVES: I. Determine patient level verified detection rates (by histopathology or a surrogate standard of truth \[second contemporaneous imaging, treatment response/change in subsequent imaging\]). II. Determine change in management plan based on POSLUMA scan (major / minor). EXPLORATORY OBJECTIVE: I. Determine patient and patient disease characteristics consistent with a positive POSLUMA scan at prostate specific antigen (PSA) \< 0.5ng/ml (i.e. pathological Gleason grade, PSA at scan, time to biochemical recurrence \[BCR\], prostate-specific antigen doubling time \[PSADT\]). OUTLINE: Patients receive rhPSMA-7.3 intravenously (IV) and undergo PET/CT 60 minutes later on day 1. After completion of study intervention, patients are followed up at 14 days and then every 3 months for 2 years.

Conditions

• Biochemically Recurrent Prostate Carcinoma
• Prostate Adenocarcinoma

Interventions

Type	Name	Description
PROCEDURE	Computed Tomography	Undergo PET/CT
OTHER	Electronic Health Record Review	Ancillary studies
OTHER	Flotufolastat F-18 Gallium	Given IV
PROCEDURE	Positron Emission Tomography	Undergo PET/CT

Timeline

• Start date: 2025-02-17
• Primary completion: 2027-02-01
• Completion: 2032-02-01
• First posted: 2025-02-07
• Last updated: 2025-02-18

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated drug study