Phase 1 Multiple Sclerosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You must be 18 years of age or older, but younger than 90
- You must be able to understand the study information and agree to take part by signing a consent form
- You must be in good general health
Who may not be able to join:
- You are under 18 years of age
- You are currently pregnant or breastfeeding
- You have a serious ongoing illness or a medical condition that is not stable or well-controlled
- You have certain pre-existing medical conditions, or you experience anxiety or panic in enclosed spaces (such as a scanner) (confirm with trial site)
- You have had a significant amount of radiation exposure from research studies in the past 12 months (confirm with trial site)
- You have a history of a bleeding disorder, or you are currently taking blood-thinning medication
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Georges El Fakhri, PhD, DABR, Yale University
Phone: +1 (203) 737-5278
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Tracers volume of distribution (VT); Distribution volume ratio (DVR); Binding potential (BPND); Demyelination; Tau burden; Amyloid burden; Tracer rate constant; Associations between imaging modalities and biomarkers.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.