CClinicalTrials.gg
RecruitingNCT06850545KuPSMALuUpdated Feb 27, 2025

Kuopio Lutetium-177 Study in Patients with PSMA-Positive Metastatic Prostate Cancer

An observational study in Metastatic Prostate Adenocarcinoma and PSMA PET-Positive Castration-Resistant Prostate Cancer, sponsored by Kuopio University Hospital. Recruiting at 1 site in Finland. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-27.

Sponsored by Kuopio University Hospital · Observational

From the registry’s dates

  • Started Jan 2020; still recruiting 6 years 8 months later.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
Male
01

Study summary

KuPSMALu-trial is an observational study for patients treated with 177LuPSMA-I\&T in Kuopio University Hospital, Finland. Study focuses on efficacy, safety and biomarker research.

02

Conditions studied

  • Metastatic Prostate Adenocarcinoma
  • PSMA PET-Positive Castration-Resistant Prostate Cancer

Browse trials for

03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's planned enrollment of 150 is below the median of 200 across 1,181 observational studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Kuopio University Hospital is the lead sponsor of 132 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

mCPRC patients treated with 177LuPSMA-I\&T in Kuopio University Hospital.

Inclusion criteria

  1. The patient must sign informed consent to participate in the study.
  2. Patients must be over 18 years of age.
  3. Patients must have histologically confirmed metastatic prostate adenocarcinoma. Histological samples may show neuroendocrine features, but the primary component must be adenocarcinoma.
  4. Patients must have metastatic castration-resistant prostate cancer (mCRPC) that has been treated with at least docetaxel and abiraterone or enzalutamide, or the patients must have declined chemotherapy or be ineligible for docetaxel-based chemotherapy due to contraindications.
  5. Patients must have an adequate performance status: WHO 0-2.
  6. Castration must have been achieved either chemically (LHRH analog or antagonist) or surgically (orchiectomy). Castration is defined as a low testosterone level (S-testosterone ≤ 1.7 mmol/l).
  7. Patients must have PSMA-positive tumor burden detected by 18F-PSMA-PET-CT imaging.
  8. Patients must have adequate renal and liver function (Creatinine \< 2x upper limit of normal (ULN), ALT and ALP \< 5x ULN).
  9. Patients' blood counts must be within acceptable levels (Hb ≥ 100 g/l, Platelets ≥ 100 x 10⁹/L, Leukocytes ≥ 3.0 x 10⁹/L, or Neutrophils ≥ 1.0 x 10⁹/L).
  10. The expected survival must be more than 6 months.
  11. Patients with ejaculatory capacity must commit to not donating sperm during the treatments and for 6 months after treatment completion.

Exclusion criteria

Exclusion Criteria:

  1. Patients whose physical condition and cooperation are insufficient to follow the given instructions.
  2. Patients who do not meet the criteria mentioned in the inclusion criteria.
  3. Patients must not have PSMA-negative tumor burden in the liver. The amount of PSMA-negative tumor burden must not exceed the amount of PSMA-positive tumor burden.
  4. Patients with symptomatic untreated spinal cord compression.
  5. Patients must not have acute hydronephrosis or urinary tract obstruction.
  6. Patients must not have a recurrent infection that impairs functional capacity.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
150 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Overall survival

    Overall survival in the trial

    Time frame: 5 years

Secondary outcomes

  1. PSA decrease of 50% or more

    PSA decrease of 50% or more within the treatment period

    Time frame: 36 weeks

  2. Adverse Events

    Treatment-related grade ≥3 and serious adverse events

    Time frame: 36 weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06850545
Lead sponsor
Kuopio University Hospital
Collaborators
University of Eastern Finland
Responsible party
Okko Kääriäinen (Clinical oncologist, Kuopio University Hospital) — Principal investigator
First posted
Feb 27, 2025
Start date
Jan 10, 2020
Primary completion
Dec 31, 2030 (estimated)
Completion
Dec 31, 2035 (estimated)
Last update
Feb 27, 2025

Study contacts

Okko-Sakari Kääriäinen, MD
Contact
okko.kaariainen@pshyvinvointialue.fi
+358447179433

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion