Precision medicine approach for high-risk prostate cancer
Official title: Swedish Prostate Cancer Initiative for Novel Treatment Regimens - Real, Implementation of Precision Medicine in High-risk Prostate Cancer
Run by Region Västerbotten · NCT06687421 · Data updated 2026-11-12
This study is trying to understand the biology of high-risk prostate cancer by collecting samples and information from patients to find better treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 5500 (estimated) |
| Sponsor | Region Västerbotten Government |
| Locations | 1 site (Umeå) |
| Status | Recruiting |
| Started | June 10, 2024 |
| Main results expected | December 2054 |
| Study ends | December 2054 |
| Registry record updated | September 3, 2025 |
| Trial ID | NCT06687421 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are men being investigated for suspected prostate cancer who can provide informed consent.
✕Probably not a fit
Patients who have difficulties understanding the study information due to linguistic or cognitive reasons 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 perform comprehensive molecular characterization and subtyping of primary tumors in patients with high-risk or metastatic prostate cancer. It involves collecting biological samples such as urine and blood, alongside health economic data and patient questionnaires. The study will also link clinical variables and molecular diagnostic outcomes to identify potential candidates for further clinical trials and to enhance the national medical information system for prostate cancer. Ultimately, it seeks to prioritize biomarkers for developing predictive treatment algorithms.
Why it matters
Potential benefit: If successful, this study could lead to more personalized and effective treatment strategies for patients with high-risk prostate cancer.
How similar studies have gone: Other studies focusing on molecular characterization in cancer have shown promise, indicating that this approach could yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Men investigated for suspected prostate cancer * Signed consent form Exclusion Criteria: * Difficulties understanding information about the study due to linguistic, cognitive or other reason
Where it's running
-
Urology, Umeå University Hospital, Region Västerbotten
Umeå, Sweden Recruiting
Study contacts
- Study coordinator: Andreas Josefsson, MD, PhD
- Email: andreas.josefsson@umu.se
- Phone: +46 907850000
Similar studies
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Salvage high-dose-rate brachytherapy for locally recurrent prostate cancer
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Multi-peptide Vaccination and PSMAxCD3 Antibody Therapy for Prostate Cancer with Biochemical Recurrence
This phase 2 trial tests whether a PSMA-targeted bispecific antibody (CC-1), a prostate cancer peptide vaccine (VAC-XS15-PC01), or both can be given safely and help control biochemical recurrence after local therapy in men with prostate cancer.
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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.