Clin2
NCT04925349Possibly a fitRecruiting

Study blood immune patterns in several rare brain diseases

AdrenoleukodystrophyAdrenomyeloneuropathyMetachromatic LeukodystrophyAdult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia

Treatments studied

Part of Brain & nervous system, Genetic & congenital, Hormones & metabolism clinical trials.

This study looks at immune cells in blood to better understand rare brain conditions caused by genetic changes. It may help researchers understand why symptoms happen and how the immune system is involved.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
1.3 years to 60 years
Study type
Observational

Who can take part

  • You (or your child) must have a specific diagnosis, such as X-linked CALD, MLD, ALD variants, or a related genetic “PRE-” stage
  • Age must match one of the study groups: about 15 months to 18 years, or 18 to 60 years
  • For “presymptomatic” groups, you carry the matching gene change but may not yet have symptoms
  • You must be able to provide blood samples (and have blood counts acceptable to the study doctor)
  • You must not be in another treatment-focused clinical trial

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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