Actively Recruiting

Phase 1
Age: 18Years +
All Genders
NCT07116486

A Trial Utilizing 18F-FS PG PET to Guide Therapy in Hepatocellular Carcinoma

Led by M.D. Anderson Cancer Center · Updated on 2026-02-19

60

Participants Needed

1

Research Sites

343 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To evaluate the relationship between 18F-FSPG uptake in HCC lesions, ctDNA in blood and clinical response to Y90 radioembolization therapy in patients with hepatocellular carcinoma (HCC) by SOC imaging.

CONDITIONS

Official Title

A Trial Utilizing 18F-FS PG PET to Guide Therapy in Hepatocellular Carcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of hepatocellular carcinoma (HCC) with at least one of the following: liver mass with non-rim arterial phase hyperenhancement (APHE) and additional major features based on LI-RADS criteria; lesions meeting LI-RADS 4 or 5 criteria; suggestive imaging plus Alpha Fetoprotein (AFP) > 200 mg/dL; tumor confirmed by arteriography; or pathologic confirmation of tumor.
  • Candidates for Y90 radioembolization monotherapy.
  • Completed conventional imaging and staging including CT before investigational PET studies.
  • Age 18 years or older.
  • Women and men of child-bearing potential must agree to use adequate contraception during the study and per MD Anderson Pregnancy Assessment Policy.
  • Ability to understand and sign informed consent.
Not Eligible

You will not qualify if you...

  • Under 18 years of age.
  • Not candidates for Y90 radioembolization monotherapy.
  • Pregnant or breastfeeding.
  • Poorly controlled diabetes mellitus (fasting blood glucose > 200 mg/dL).
  • Psychiatric illness or social situations limiting study compliance.
  • Not recovered from adverse events or allergic reactions to similar compounds.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

S

Simone Krebs, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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