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Clinical Trials in the EU / 2025-522768-33-00
Completed Phase II

Is [18F]-DPA-714 PET a good marker of neuroinflammation in autoimmune encephalitis? (EAI-714)

2025-522768-33-00 · tracked via the Priya Life Science EU tracker
Sponsor
Centre Hospitalier Universitaire De Toulouse
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Nervous System Diseases
Decision date
15/12/2025
Enrollment target
20
Sites
France

Condition studied

autoimmune encephalitis

Investigational medicinal product(s)

18F-DPA-714

Eligibility

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

Primary endpoint

The primary endpoint will be the value of the «Binding Potential» (BP) of DPA-714 at the whole brain scale calculated by an automated clustering method in supervised cluster analysis (SVCA).

Endpoint detail

The BPs of regions of interest will be compared between patients and controls., The result of imaging [18F]-DPA-714 in PET will be, for each participant, dichotomized into 2: positive and negative. A result will be classified as "positive" if at least one region of interest has a BP greater than 2-DS compared to the average of control participants as done in the study by Zhang et al., 2024. The percentage of patients with a positive result will be calculated., The results of other biomarkers conventionally used for the diagnosis of AIE will also be divided into 'positive' and 'negative'. Patients will be classified into positive/negative according to each biomarker to identify the most effective biomarker., Finally, a linear regression analysis will be performed between the overall BP of patients and clinical severity scores, We will make a description of a possible concordance between the BP by region of interest and the presence of identified symptoms

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 2025-522768-33-00 on CTIS ↗ ← All trials in the EU