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NCT06389097Recruiting

SPECT Imaging for Pharmacokinetics and dosimEtry Towards TREATment Optimization

Single-Photon Emission Computed Tomography (SPECT) Imaging for Pharmacokinetics and dosimEtry Towards TREATment Optimization (SEEtoTREAT)

Source: ClinicalTrials.gov · Last updated 30 Mar 2026

Brief summary (registry, in English)

The investigators will study SPECT imaging of radiopharmaceutical therapies given as standard of care or as part of other compatible research protocols. The goal is to validate the quantitative SPECT image reconstruction methods developed in this proposal, and to investigate the relation between dosimetry calculated from SPECT images and the outcomes. Patients will be recruited for SPECT/CT imaging during treatment. This is an observational study no additional new drugs or activities will be administrated. The investigators will perform SPECT imaging on a total of 80 patients (\~20 each from year 2 to year 5). Each participant will be imaged 3 times after the first and last cycles of planned radiopharmaceutical therapy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
80 (estimated)
First submitted
24 Apr 2024
Start date
3 Feb 2025
Primary completion date
30 Nov 2028
Lead sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
NCT number
NCT06389097

What you commit to

  • Study type: Observational
  • Planned participants: 80
  • From 3 Feb 2025 to the primary completion date, 30 Nov 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patient is participating in another research protocol that does not allow participation in this imaging protocol or that has schedule of procedures that would not be compatible with this protocol.
  • Patient unable to tolerate SPECT scan time, scan frequency, or position.

Who the study is looking for

  • Cohort A: Patients with advanced prostate cancer planning to undergo treatment with Radium-223
  • Cohort B: Patients with advanced cancer undergoing treatment with 177Lu-DOTATATE or 177Lu-PSMA-617
    • \*\*Eligible patients may be planning to undergo these treatments as part of standard of care or as part of another research protocol
  • Age \> 18 years
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • Histologic confirmation of malignancy

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.