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RECRUITING
NCT06815354
NA

Comprehensive Assessment of Cancer Theranostic Response

Sponsor: AIQ Solutions

View on ClinicalTrials.gov

Summary

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.

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

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2024-12-02

Completion Date

2026-05-29

Last Updated

2025-09-09

Healthy Volunteers

No

Conditions

Interventions

DEVICE

TRAQinform Theranostics

This prospective, multi-center, non-interventional clinical study will evaluate actionable outputs from TRAQinform Theranostics, a software only medical device that identifies, quantifies, tracks, and compares lesions between different imaging modalities and multiple imaging timepoints.

Locations (2)

Weill Medical College of Cornell

New York, New York, United States

M.D. Anderson Cancer Center

Houston, Texas, United States