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NCT06815354Active, not recruiting

Comprehensive Assessment of Cancer Theranostic Response

Comprehensive Assessment of Cancer Theranostic Response; Investigating the Intent to Change Treatment Decisions Based on TRAQinform Theranostics

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

The intent of this study is to evaluate actionable outputs from TRAQinform Theranostics in a prospective, multi-center, non-interventional clinical study. The primary objective is to investigate intent-to-change treatment decisions after the addition of TRAQinform Theranostics. The exploratory objective is to investigate if treatment efficacy and treatment-related toxicity could be detected by TRAQinform Theranostics following PSMA PET/CT at week 12.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
25 (actual)
First submitted
4 Feb 2025
Start date
2 Dec 2024
Primary completion date
31 Aug 2026
Lead sponsor
AIQ Solutions
NCT number
NCT06815354

What you commit to

  • Study type: Interventional
  • Participants enrolled: 25
  • From 2 Dec 2024 to the primary completion date, 31 Aug 2026
  • 2 sites 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.

Prior treatment

  • Any concurrent disease, infection, or comorbid condition that interferes with the ability of the patient to participate in the trial.

Who the study is looking for

  • Age 18 years or older and willing and able to provide informed consent.
  • Diagnosis of metastatic prostate cancer.
  • Planned to start 177Lu-PSMA (Pluvicto).
  • Ability to tolerate two 68Ga-PSMA or 18F-DCFPyL PET/CT imaging procedures. One at baseline and at 12 weeks of 177Lu-PSMA (Pluvicto) treatment.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2 at screening.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
M D Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Weill Medical College of Cornell
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

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