Collecting data on prostate cancer patients treated with Lu-PSMA therapy
Official title: Data Collection in Lutetium Treated Prostate Cancer: Recording of Progression and Tumor Characteristics
Run by Erasmus Medical Center · NCT06260410 · Data updated 2026-11-12
This study is trying to learn more about how well Lu-PSMA therapy works for men with advanced prostate cancer by collecting data and blood samples from patients receiving the treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 150 (estimated) |
| Sponsor | Erasmus Medical Center Academic / other |
| Locations | 1 site (Rotterdam, South Holland) |
| Status | Recruiting |
| Started | February 20, 2024 |
| Main results expected | February 1, 2027 |
| Study ends | February 1, 2027 |
| Registry record updated | April 22, 2024 |
| Trial ID | NCT06260410 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who are about to start Lu-PSMA treatment as part of their clinical care.
✕Probably not a fit
Patients who are not starting Lu-PSMA therapy or are under 18 years old may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to gather data and blood biomarkers from patients receiving Lu-PSMA therapy for metastatic prostate cancer at Erasmus MC. By collecting real-world efficacy and safety data, the study seeks to understand the treatment's impact and identify potential biomarkers that could predict which patients benefit the most. Participants will undergo blood draws for ctDNA and circulating tumor cell collection as part of the data collection process.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of Lu-PSMA therapy's effectiveness and safety, leading to improved patient selection and outcomes.
How similar studies have gone: While this study focuses on real-world data collection, similar approaches in other studies have shown promise in understanding treatment efficacy and safety.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants should be at least 18 years old. * Participants should be able to understand the written information and be able to provide informed consent. * Participants are planned to start treatment with Lu-PSMA as a part of regular clinical care. Exclusion Criteria: None applicable
Where it's running
-
Erasmus MC
Rotterdam, South Holland, Netherlands Recruiting
Study contacts
- Study coordinator: Stijn Koolen, PhD
- Email: s.koolen@erasmusmc.nl
- Phone: +31638740656
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.