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NCT06220435

Tumor-directed Radiation Therapy for Patients With the Highest Risk Category of Localized Prostate Cancer

Recruiting now NA Last updated 12 August 2025
What this trial tests

NA trial testing Ultra-hypofractionated radiotherapy regimen. in Prostate Cancer in 76 participants. Currently enrolling.

Timeline
25 September 2023
Primary endpoint
1 September 2031
1 September 2031

Quick facts

Lead sponsorRegion Skane
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment76
Start date25 September 2023
Primary completion1 September 2031
Estimated completion1 September 2031
Sites2 locations across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Region Skane — full company profile →

Who can join

18 and older, male only, with Prostate Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

HYPO-RT-PC boost is is an open-label, multicentre, phase II trial evaluating safety and efficacy of real-time image-guided tumor-directed ultra-hypofractionated radiation boost and lymph node irradiation for patients with node-negative high risk localized prostate cancer.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Ultra-hypofractionated radiotherapy with focal boost for high-risk localized prostate cancer (HYPO-RT-PC-boost): in silico evaluation with histological reference.
    Nilsson E, Nilsson A, Jonsson J, Sandgren K, et al · · 2025 · PMID 41146436 · DOI 10.2340/1651-226x.2025.44211

Verify or expand the search:

Other recruiting trials for Prostate Cancer

Currently open trials in the same condition.

Other Region Skane trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06220435.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing