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Clinical Trials in the EU / 2025-521163-12-01
Authorised Phase I/II

The use of [68Ga]Ga-FAPI PET/MRI in assessing disease activity in patients with Graves’ orbitopathy

2025-521163-12-01 · tracked via the Priya Life Science EU tracker
Sponsor
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Immune System Diseases
Decision date
30/10/2025
Enrollment target
10
Sites
Netherlands

Condition studied

Graves' Orbitopathy

Investigational medicinal product(s)

68GA-FAPI-46

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

FAPI uptake in active GO versus inactive GO on PET-MRI

Endpoint detail

Relation MRI results (edema), clinical symptoms, and lab values to FAPI-uptake on PET.

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-521163-12-01 on CTIS ↗ ← All trials in the EU