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LuTACT

Research Topic: Prostate Cancer

Study Title: Comparison of 177Lu-PSMA-617 and 225Ac-PSMA-617 in a Prostatectomy Model (LUTACT Trial)

Research Team:
Thomas Hope, MD, Principal Investigator (PI)
Jose Garcia, Clinical Research Coordinator

Sponsor: Novartis

Who can join?

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  • Histologically confirmed prostate adenocarcinoma
  • Willing to undergo prostatectomy with or without lymph node dissection, and candidate for prostatectomy as determined by urologic oncology.
  • High risk disease as defined as meeting 1 or more of the 3 following criteria: 
    1. Gleason 4+5 disease or higher 
    2. Pelvic nodal metastases on PSMA PET 
    3. Extracapsular extension or seminal vesicle invasion on MRI No evidence of distant metastatic disease as determined by PSMA PET. Nodal disease below the iliac bifurcation (clinical stage N1) is allowed. 
  • Maximum Standardized Uptake Value (SUVmax) in the primary tumor greater than 10 on PSMA PET using 68Ga-PSMA-11 or 18F-DCFPyL. 
Red X
  • Has received prior prostate cancer therapy. 
  • Prior 5-alpha reductase inhibitors (e.g. finasteride, dutasteride) allowed if discontinued at least 3 weeks prior to treatment start

What to Expect During the Study

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Research activities

Undergoing treatment and 2-3 research scans, several research blood collections, surveys, physician visits.

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Location

In person only

UCSF Mission Bay campus
UCSF China Basin

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How you can help
  • Participation in this study will help researchers compare two radioligand therapies to better understand which treatment delivers more radiation to prostate tumors, how they affect cancer cell death, and how they interact with the immune system. 
  • The knowledge gained may help improve treatment options for future patients with high-risk prostate cancer.

FAQ's

60 months

Visits at screening, Cycle 1 Day 1, 2, 8, and 22, and day of as well as day prior to prostatectomy. Follow ups at Day 42 as well as 6 additional visits up to 60 months after Cycle 1, Day 1.

Up to $300

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