Blood markers may unlock early ALS detection — a study puts them to the test
NCT ID NCT07737977
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
ALS is a progressive nerve disease with no simple test for early diagnosis or tracking. This study is collecting blood samples and medical data from 200 people with ALS to look for patterns in proteins, genes, and immune markers. The goal is to build a biomarker panel that could one day help doctors diagnose ALS sooner and predict how the disease will progress.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a blood test that helps diagnose ALS earlier and predict how the disease will progress.
- What could go wrong
- This is an observational study, not a treatment trial. It may not identify a useful biomarker panel, and results may take years to apply in clinical practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult participants with amyotrophic lateral sclerosis (ALS) meeting the El Escorial diagnostic criteria. Both sporadic and familial ALS cases, including spinal-onset and bulbar-onset phenotypes, are eligible for participation. Participants will be recruited at Montpellier University Hospital, a specialized ALS center, and will provide blood samples and clinical data for biomarker analyses.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age greater than 18 years. * Male and female patients with ALS diagnosed according to the El Escorial diagnostic criteria. * Sporadic or familial ALS cases. * Spinal-onset or bulbar-onset ALS cases. Exclusion Criteria: * Refusal to participate. * Individuals deprived of liberty (Article L1121-6), including those subject to judicial or administrative decisions or involuntary hospitalization. * Adults under legal protection (guardianship, curatorship, or judicial protection measures) (Article L1121-8). * Individuals not affiliated with, or not beneficiaries of, a French social security scheme (Article L1121-8-1). * Individuals participating in another research study with an ongoing exclusion period (Article L1121-12).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Universitari Vall D'Hebron
Barcelona, 08035, Spain
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Montpellier University Hospital
Montpellier, Occitanie, 34295, France
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