68Ga PSMA in Preprostatectomy Patients
NCT03388346 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 22
Last updated 2024-02-15
Summary
This study investigates if a new drug (PSMA) makes prostate cancer easier to identify in positron-emission tomography (PET) imaging. If this works, prostate cancer treatments can be prescribed that match the location of the disease. PSMA is radiolabeled with Gallium-68 (Ga-68). This means a participant receives a small dose of radiation from the drug - less than the annual radiation limit for a medical worker.
To test this new drug, participants will receive an injection of Ga-68 PSMA and then have a PET scan. This PET scan, and the reported results, will be entered into the medical record and shared with the treating oncologists.
Conditions
- Prostate Cancer
- Prostatic Neoplasm
- Prostatic Neoplasms, Castration-Resistant
- Prostatic Neoplasm of Uncertain Behavior
Interventions
- DRUG
-
Ga-68 PSMA-HBED-CC PET
Ga-68 PSMA-HBED-CC is an investigational PET drug (radionuclide), that binds to the prostate specific receptors. The dose will be about 5mCi (range 3-7 mCi) and administered intravenously.
Sponsors & Collaborators
-
Holden Comprehensive Cancer Center
collaborator OTHER -
University of Iowa
collaborator OTHER -
Michael Graham PhD, MD
lead OTHER
Principal Investigators
-
Michael Graham, MD, PhD · University of Iowa
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-02-16
- Primary Completion
- 2021-07-22
- Completion
- 2021-07-22
- FDA Drug
- Yes
Countries
- United States
Study Locations
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