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Study identifier: NCT06706921 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

18F-Fluciclovine PET/CT Impact on Predicting Clinical Outcome of 177Lu-PSMA-617 Therapy in Patients With Prostate Cancer

Condition: Prostatic Neoplasms · Prostatic Neoplasms, Castration-Resistant · Metastatic Prostate Cancer  ·  Sponsor: VA Greater Los Angeles Healthcare System

PhasePhase 4
Planned participants15
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This a single-center, prospective, exploratory study. Patients with metastatic castration-resistant prostate cancer (mCRPC) scheduled to undergo Lutetium labelled prostate-specific membrane antigen radioligand therapy (LuPSMA RLT) at the West Los Angeles VA (WLA-VA) will be imaged with a baseline F-18 fluorodeoxyglucose positron emission tomography/computed tomography 18F-FDG PET/CT and a 18F-DCFPyL PET/CT (18F-DCFPyL (2-(3-{1-carboxy-5-\[(6-18F-fluoro-pyridine-3-carbonyl)-amino\]-pentyl}-ureido)-pentanedioic acid)positron emission tomography/computed tomography , as per standard of care in our institution. All patients further undergo eventual follow-up prostate-specific membrane antigen positron emission tomography (PSMA PET) after the 2nd, 4th, and 6th LuPSMA RLT cycle. In this prospective study, an18F-Fluciclovine positron emission tomography/computed tomography ( Axumin PET/CT )will be additionally obtained at baseline (pre-LuPSMA RLT), and after the 2nd, 4th, 6th LuPSMA RLT cycles. Axumin PET/CT will be acquired within 7 days from the PSMA PET. This study is open to Veterans only.

This description comes directly from the study's public registry record.

Talk to the study team

Gholam Berenji, MD  ·  310-268-3547  ·  Gholam.Berenji@va.gov

Janake Wijesuriya, BS  ·  310-977-5209  ·  Janake.Wijesuriya@va.gov

Always discuss trial participation with your own doctor first.

Locations (1)

VA Greater Los Angeles Healthcare SystemLos Angeles, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06706921