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Study details
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Vorinostat and 177Lu-PSMA-617 for Prostate Cancer

Fred Hutchinson Cancer Center
NCT IDNCT06145633ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

15

Study length

about 3.3 years

Ages

All ages

Sex

Male only

Locations

1 site in WA

What this study is about

Researchers are testing how well vorinostat works in treating patients with prostate cancer that has spread to other parts of the body. This treatment involves a biopsy procedure, biospecimen collection, bone scan, computed tomography, fludeoxyglucose F-18, gallium Ga 68 gozetotide, lutetium Lu 177 vipivotide tetraxetan, positron emission tomography, and single photon emission computed tomography. The trial will last for about 1198 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Fludeoxyglucose F-18
  • 2.Gallium Ga 68 Gozetotide
  • 3.Take Lutetium Lu 177 Vipivotide Tetraxetan
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

fludeoxyglucose (18F), gallium (68Ga) gozetotide, lutetium (177Lu) vipivotide tetraxetan, vorinostat

Drug routes

oral (Oral Capsule)

Endpoints

Secondary: Absolute change in PSMA standardized uptake value (SUV) mean, Incidence of adverse events, Objective radiographic response rate, Overall survival, PSA PFS, Progression free survival (PFS), Prostate specific antigen (PSA)50 response rate

Procedures

biopsy, diagnostic, imaging

Body systems

Oncology