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NCT06520345 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study of Metastatic Castration-Resistant Prostate Cancer, sponsored by Telix Pharmaceuticals (Innovations) Pty Limited.

Recruiting
Registry status
Phase 3
Development phase
430
Enrollment target
15
Study locations

NCT06520345: Recruiting Phase 3 study of Metastatic Castration-Resistant Prostate Cancer, sponsored by Telix Pharmaceuticals (Innovations) Pty Limited.

NCT06520345 is a Phase 3 study of Metastatic Castration-Resistant Prostate Cancer that is actively recruiting participants, run by Telix Pharmaceuticals (Innovations) Pty Limited. The registered enrollment target is 430 participants, above the 192-participant average among 69 other Metastatic Castration-Resistant Prostate Cancer trials with a reported enrollment target (124% higher). The trial reports 15 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06520345, a Phase 3 study of Metastatic Castration-Resistant Prostate Cancer, is actively recruiting participants, sponsored by Telix Pharmaceuticals (Innovations) Pty Limited.

RECRUITING
Registry status
Phase 3
Development phase
430 participants
Enrollment target
15
Study locations

Study Summary

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

Primary Outcome

time from randomization to disease progression confirmed by central independent radiology review according to Prostate Cancer Clinical Trials Working Group 3 (PCWG3) criteria (which incorporates Response Evaluation Criteria in Solid Tumors, RECIST 1.1, for soft tissue lesions), or death (whichever occurs first)

Interventions

  • DRUG Docetaxel
  • DRUG Enzalutamide
  • DRUG Abiraterone
  • DRUG 177Lu-TLX591

Study Locations (15)

New South Wales

  • Westmead Hospital - Sydney
  • Nepean Hospital - Sydney
  • Wollongong Hospital - Wollongong

Utah

  • Intermountain Health - Murray
  • Intermountain Health - Salt Lake City

California

  • Chao Family Comprehensive Cancer Centre - Orange

Florida

  • Biogenix Molecular LLC - Miami

Maryland

  • United Theranostics - Glen Burnie

Nebraska

  • XCancer Omaha - Omaha

New York

  • Columbia University Herbert Irving Comphrensive Cancer Center - New York

Ohio

  • University Hospital - Cleveland

Trial Details

FieldValue
Enrollment Target 430 participants
Start Date 2024-07-26
Est. Completion 2030-12
Phase Phase 3

What NCT06520345 shows while recruiting

NCT06520345 is an interventional study that assigns participants to a tested intervention. The registered 430 participants enrollment target is mid-sized for trials with a published cap, above the 192-participant average among 69 other Metastatic Castration-Resistant Prostate Cancer trials with a reported enrollment target (124% higher).

The record links to 1 condition, with Metastatic Castration-Resistant Prostate Cancer appearing as the primary indexed condition, and to 4 interventions - of which Docetaxel is the first listed.

NCT06520345 lists 15 locations in 12 states (New South Wales, Utah, California).

Frequently Asked Questions

What is clinical trial NCT06520345 about?

NCT06520345 is a clinical study titled "The Study of 177Lu-TLX591 Plus SOC Versus SOC Alone in Patients With mCRPC (ProstACT Global)". 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

What is the current status of trial NCT06520345?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 430 participants. The study started on 2024-07-26. Estimated completion is 2030-12.

What conditions does trial NCT06520345 study?

This clinical trial studies the following conditions: Metastatic Castration-Resistant Prostate Cancer.

What interventions are being tested in trial NCT06520345?

The interventions under investigation include: Docetaxel (DRUG), Enzalutamide (DRUG), Abiraterone (DRUG), 177Lu-TLX591 (DRUG).

Who is sponsoring clinical trial NCT06520345?

This trial is sponsored by Telix Pharmaceuticals (Innovations) Pty Limited, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06520345 being conducted?

This trial has 15 study locations across California, Florida, Maryland, Nebraska, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Metastatic Castration-Resistant Prostate Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06520345's enrollment target sits among peer trials

430 10th of 69 higher than 60 of 69 other Metastatic Castration-Resistant Prostate Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Metastatic Castration-Resistant Prostate Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06520345, the US trial registry maintained by the National Library of Medicine. NCT06520345 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.