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NCT06280742RecruitingPhase 2/3

INFLANET - A French Network for PET imaging of neuroinflammation in MS

Source: EU CTIS (euclinicaltrials.eu) · Last updated 13 Aug 2026

Brief summary (registry, in English)

To quantify, in a multicentre trial applying [18F]-DPA-714 PET, the smoldering component of white matter lesions in people with multiple sclerosis (PwMS), as compared with [18F]-DPA-714 binding in the white matter of healthy controls who underwent a PET acquisition with the same camera than patients in each center.

Status (registry)
Recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
66 (estimated)
First submitted
1 Mar 2024
Start date
16 Dec 2025
Lead sponsor
Assistance Publique Hopitaux De Paris
NCT number
NCT06280742
EU CT number
2023-510304-53-00

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 66
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Lab values

  • all participants: - Any reasons, which does not allow to perform MRI, including claustrophobia, the implant of a pace-maker or the presence of an intra-ocular foreign body, (a contra-indication questionnaire will be filled in beforehand) - PET for clinical research already done within the last 12 months - Low Affinity Binding profile (analyse of TSPO polymorphism done at screening visit) - Pregnancy, breast-feeding, lack of efficient contraception for women of childbearing potential - Current symptoms of severe or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary or cardiac disease, or any other chronic neurological diseases - Unwillingness to be informed in case of unexpected MRI abnormality (with a significant medical anomaly) - Patient under legal protection - Participation in another interventional study or being in the exclusion period at the end of a previous study RRMS patients: - hypersensitivity to gadoteric acid - meglumine or any drug containing gadolinium - Severe renal insufficiency (creatinine clearance < 60mL/min and GFR <30ml / min / 1.73m2).

Who the study is looking for

  • RRMS patients: - Age between 18 and 55 years old - RRMS according to the 2017 Mc Donald criteria - Last treatment with methylprednisolone should have been performed at least 1 month before PET examinations - No current disease modifying therapy or under platform therapy (dimethyl fumarate, teriflunomide, beta-interferons, glatiramer acetate)- Indication for a highly active disease modifying treatment: Natalizumab, anti CD20 antibody, Alemtuzumab, sphingosine-1 phosphate modulator, or cladribine. This will consist either as patients with an active form of relapsing MS or patients who have experienced two relapses during the previous year - Affiliation to a social security scheme or beneficiary of such a scheme (except “Aide Médicale d’Etat”) Healthy Volunteers: - Age between 18 and 55 years old - Without any evolutive pathology - Able to understand the study objectives and procedures - Affiliation to a social security scheme or beneficiary of such a scheme (except “Aide Médicale d’Etat”)

Age in the registry: 18 years to 64 years · Sex: All · Accepts healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (7)

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

SiteCityCountrySite status
Hospices Civils de Lyon
Coordinator of this site? Confirm its status
BronFranceRecruiting
Commissariat A L'energie Atomique Et Aux Energies Alternatives
Coordinator of this site? Confirm its status
Orsay CedexFranceRecruiting
Assistance Publique Hopitaux De Paris
Coordinator of this site? Confirm its status
Paris Cedex 13FranceRecruiting
Centre Hospitalier Universitaire de Rennes
Coordinator of this site? Confirm its status
RennesFranceRecruiting
Centre De Lutte Contre Le Cancer Eugene Marquis
Coordinator of this site? Confirm its status
Rennes CedexFranceRecruiting
Centre Hospitalier Universitaire de Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceRecruiting
CHRU De Nancy
Coordinator of this site? Confirm its status
Vandoeuvre Les NancyFranceRecruiting

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