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NCT07007208RecruitingPhase 2

Biomarkers of the Locus Coeruleus Nucleus: Links With Early Tau Pathology, Cognition and Alzheimer's Disease Risk

Biomarkers of the Locus Coeruleus Nucleus: Links With Early Tau Pathology, Cognition and Alzheimer's Disease Risk.

Source: ClinicalTrials.gov · Last updated 17 Jul 2026

Brief summary (registry, in English)

Alzheimer's disease (AD) is characterized by a long-lasting silent phase. Among initial events, emergence of tau pathology in locus coeruleus (LC) brainstem nucleus, well before the one observed in medial temporal cortex, is highly relevant. LC integrity and function can be assessed in vivo with MRI and pupil measures. The current research proposes to evaluate these LC markers in an aged healthy cohort (n=100, with half APOE4 positive) and to relate these markers with cerebral tau pathology, AD risk and cognitive function.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
First submitted
12 May 2025
Start date
2 Feb 2026
Primary completion date
31 Jan 2029
Lead sponsor
University Hospital, Toulouse
NCT number
NCT07007208
EU CT number
2023-507668-38-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 100
  • From 2 Feb 2026 to the primary completion date, 31 Jan 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects with a psychiatric disorder and a PHQ-9 score \> 10 or under treatment with NRI

Other illness

  • Subjects with a known allergic reaction to the PET radiopharmaceutical (\[18F\] Flortaucipir) or any of its excipients
  • Subjects with a neurodegenerative condition or a history of cerebral ischemia

Other

  • Subjects with a contraindication to MRI exam
  • Subjects with an ophthalmological pathology making oculometric measurements difficult

Who the study is looking for

  • Participant in the INSPIRE-T cohort
  • Normal cognitive assessment
  • MMSE score ≥ 27 out of 30 (Mini-Mental State Examination)
  • Normal visual abilities (in corrected or uncorrected vision)
  • Normal motor skills

Age in the registry: 60 years to 100 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital of Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.