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Recruiting Phase 3 Interventional

The Study of 177Lu-TLX591 Plus SOC Versus SOC Alone in Patients With mCRPC (ProstACT Global)

ClinicalTrials.gov ID: NCT06520345

Public ClinicalTrials.gov record NCT06520345. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 5:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multinational, Multicenter, Prospective, Randomized, Controlled, Open-Label, Phase 3 Study of Lutetium (177Lu) Rosopatamab Tetraxetan in Combination With Standard of Care Versus Standard of Care Alone in Patients With PSMA Positive Metastatic Castration-Resistant Prostate Cancer Previously After Androgen Receptor Pathway Inhibitor Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the efficacy and safety of 177Lu-TLX591 in patients with metastatic castration-resistant prostate cancer who have progressed following treatment with Androgen Receptor Pathway Inhibitor Treatment

Study identification

NCT ID
NCT06520345
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Enrollment
520 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 26, 2024 (Actual)
Primary completion
Dec 2027 (Estimated)
Completion
Dec 2030 (Estimated)
Last update posted
Jul 21, 2026

2024 – 2030

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Chao Family Comprehensive Cancer Centre Orange California 92868 Active, not recruiting
Biogenix Molecular LLC Miami Florida 33165 Active, not recruiting
United Theranostics Glen Burnie Maryland 21061 Active, not recruiting
XCancer Omaha Omaha Nebraska 68130 Active, not recruiting
Columbia University Herbert Irving Comphrensive Cancer Center New York New York 10032 Recruiting
University Hospital Cleveland Ohio 44106 Active, not recruiting
OHSU Knight Cancer Center Portland Oregon 97239 Active, not recruiting
Intermountain Health Murray Utah 84107 Active, not recruiting
Intermountain Health Salt Lake City Utah 84112 Active, not recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06520345, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2026 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06520345 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →