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NCT07116486

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

Recruiting now Phase 1 Last updated 19 February 2026
What this trial tests

Phase 1 trial testing Radiopharmaceutical 18F-FSPG in Hepatocellular Carcinoma in 60 participants. Currently enrolling.

Timeline
2 December 2025
Primary endpoint
30 June 2030
30 June 2032

Quick facts

Lead sponsorM.D. Anderson Cancer Center
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment60
Start date2 December 2025
Primary completion30 June 2030
Estimated completion30 June 2032
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

18 and older, any sex, with Hepatocellular Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hepatocellular Carcinoma

Currently open trials in the same condition.

Other M.D. Anderson Cancer Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07116486.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing