Recruiting
Phase 2

177Lu-PSMA-617

Sponsor:

Jonsson Comprehensive Cancer Center

Code:

NCT06216249

Conditions

Prostate Carcinoma

Stage IVB Prostate Cancer American Joint Committee on Cancer (AJCC) v8

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Computed Tomography

Gallium Ga 68 Gozetotide

Lutetium Lu 177 Vipivotide Tetraxetan

Positron Emission Tomography

PSMA PET Scan

Study Details

Brief summary:

In advanced metastatic castration resistant prostate cancer (mCRPC) progressing after chemotherapy and androgen receptor (AR)-targeted therapy 177Lu-PSMA-617 is an effective treatment. 177Lu-PSMA-617 RLT is administered with a fixed schedule: 6 treatment cycles, administered every 6 weeks. However, the optimum number of cycles of 177Lu-PSMA in patients who show good response remains unknown. Some patients may benefit from more than 6 cycles of therapy. Additionally, some patients experience a complete or almost complete response before the last cycle. It is unclear whether these patients benefit from the subsequent remaining treatment cycle(s). A treatment holiday period would spare these patients some exposure to the therapy agent and avoid potentially unnecessary toxicity when treatment efficacy is already maximal and additional treatment effect cannot be expected. This randomized phase 2 study compares a group of patients treated with LuPSMA on a flexible and extended dosing schedule including "treatment holiday" periods (investigational arm, up to 12 cycles, as described below) to a control group treated with a fixed dosing schedule of 6 treatments cycles maximum administered every 6 weeks. The flexible dosing schedule in the investigational arm will be based on single photon emission computed tomography (SPECT)/computed tomography (CT) response assessments obtained 24h after injection of LuPSMA therapy cycle. The response assessment during treatment holiday period will be based on positron emission tomography/computed tomography (PET/CT) every 12 weeks. Single-time point SPECT/CT dosimetry protocol at every cycle will be performed and will allow to determine the number of cycles that subjects may receive under the study without exceeding the kidney dose threshold.

Conditions

Prostate Carcinoma

Stage IVB Prostate Cancer American Joint Committee on Cancer (AJCC) v8

Study ID

NCT06216249

Start date

Aug 1, 2024

Status verified date

Mar, 2026

Completion date

Dec 31, 2028

Anticipated

Primary completion date

Dec 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patients must have prostate cancer proven by histopathology
  • Patients must have ≥ 1 metastatic lesion by any imaging (CT, magnetic resonance imaging \[MRI\], bone scan, PET)
  • Patients must have received at least one regimen of chemotherapy for mCRPC
  • Patients must have received at least one androgen-receptor signaling inhibitors (ARSI)
  • Patients must be eligible by PSMA PET VISION criteria. PSMA PET/CT must be performed within 8 weeks of planned first cycle of 177Lu-PSMA-617
  • White blood cell (WBC) ≥ 2,500/ul
  • Platelets (PLT) ≥ 100,000/ul
  • Hemoglobin (Hb) ≥ 9.0 g/dl
  • Absolute neutrophil count (ANC) ≥ 1,500 ul
  • Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
  • Patients must be adults ≥ 18 years of age
  • Patients must have the ability to understand and sign an approved informed consent form (ICF)
  • Patients must have the ability to understand and comply with all protocol requirements

Exclusion Criteria:

  • Prior cycle of 177Lu-PSMA-617 therapy
  • Less than 6 weeks between last myelosuppressive therapy (including docetaxel, cabazitaxel, strontium-89, samarium-153, rhenium-186, rhenium-188, radium-223, hemi-body irradiation) and first cycle of 177Lu-PSMA-617 therapy
  • Glomerular filtration rate (GFR) < 50 ml/min
  • Urinary tract obstruction or marked hydronephrosis

Study Design

Enrollment

90 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Arm I (177Lu-PSMA-617)

Patients receive 177Lu-PSMA-617 IV once every 6 weeks on study. Beginning with the third cycle, treatments may be postponed beyond the 6 weeks interval based on defined response criteria ("treatment holiday" period). Treatment repeats every 6 weeks for 12 cycles in the absence of disease progression or unacceptable toxicity. Patients receive 68Ga-PSMA-11 IV and undergo PSMA PET/CT throughout the trial. Patients also undergo SPECT/CT, PET/CT, or CT on the trial.

active comparator: Arm II (177Lu-PSMA-617)

Patients receive 177Lu-PSMA-617 IV once every 6 weeks on study. Treatment repeats every 6 weeks for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients receive 68Ga-PSMA-11 IV and undergo PSMA PET/CT throughout the trial. Patients also undergo SPECT/CT, PET/CT, or CT on the trial.

Interventions

Computed Tomography

Undergo PSMA PET/CT, SPECT/CT, PET/CT and CT

Gallium Ga 68 Gozetotide

Given IV

Lutetium Lu 177 Vipivotide Tetraxetan

Given IV

Positron Emission Tomography

Undergo PET/CT

PSMA PET Scan

Undergo PSMA PET/CT

Questionnaire Administration

Ancillary studies

Single Photon Emission Computed Tomography

Undergo SPECT/CT

Primary outcome measure

  • 2-year survival rate [ Time Frame: From the date of the first cycle of Lu 177 vipivotide tetraxetan (177Lu-prostate-specific membrane antigen [PSMA]-617) therapy, up to 2 years ]

Central Contacts and Locations

Central contacts

Locations

UCLA / Jonsson Comprehensive Cancer Center

Recruiting

Los Angeles, California, United States, 90095

Contacts

Principal Investigator:

Jeremie Calais

More Information

Sponsor

Jonsson Comprehensive Cancer Center

Last update posted

Mar 10, 2026

Last verified

Mar, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Jonsson Comprehensive Cancer Center on 2026-03-10.