Comprehensive Assessment of Cancer Theranostic Response

Description

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.

Conditions

Prostate Cancer

Study Overview

Study Details

Study overview

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.

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

Comprehensive Assessment of Cancer Theranostic Response

Condition
Prostate Cancer
Intervention / Treatment

-

Contacts and Locations

New York

Weill Medical College of Cornell, New York, New York, United States, 10065

Houston

M.D. Anderson Cancer Center, Houston, Texas, United States, 77030

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

MALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

AIQ Solutions,

Study Record Dates

2026-02-26