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Study identifier: NCT06687421 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingSPRINTR-REAL

Implementation of Precision Medicine in High-risk Prostate Cancer

Condition: Prostate Cancer  ·  Sponsor: Andreas Josefsson

PhaseN/A
Planned participants5500
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereUmeå, Sweden

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This project's objective is to initiate a prospective non-interventional clinical study to perform full molecular characterization and subtyping of the primary tumor prostate cancer patients. It will identify, compare, and select biomarkers for treatment response in high-risk/metastatic prostate cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Andreas Josefsson, MD, PhD  ·  +46 907850000  ·  andreas.josefsson@umu.se

Karin Welen, PhD  ·  karin.welen@urology.gu.se

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Urology, Umeå University Hospital, Region VästerbottenUmeå, SwedenRecruiting

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Umeå

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