New ALS drug shows promise in Mid-Stage trial
NCT ID NCT06365216
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new drug called NX210c in 80 adults with ALS, a nerve disease that weakens muscles over time. Participants receive multiple IV infusions of the drug or a placebo to see if it slows the disease and is safe. The main focus is on changes in blood markers that reflect nerve damage.
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.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2024
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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: * Aged ≥ 18 years, inclusive at screening. * Patients diagnosed as having possible, probable, probable laboratory-supported, or definite ALS according to El Escorial Revised criteria. * King's Clinical Staging Stage ≤3, disease duration of ≤ 36 calendar months Exclusion Criteria: * Patients with any cognitive or psychological disorder, intellectual disability or other significant impairment that would result in an inability to understand and sign the informed consent. * History of any clinically significant or unstable medical, neurological, psychiatric condition, disorder or disease (other than ALS) or social circumstances that, based on the investigator's judgment, would interfere with the conduct of the study or pose a risk to the patient if they were to participate.
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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.
Contacts and locations
Locations
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CHRU De Nancy
Nancy, France, 54000, France
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CHU de Lyon HCL
Bron, 69500, France
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Centre Hospitalier Et Universitaire de Limoges
Limoges, 87042, France
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Centre Hospitalier Regional Et Universitaire De Brest
Brest, France, 29200, France
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Centre Hospitalier Regional Universitaire de Tours
Tours, 37044, France
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Centre Hospitalier Universitaire De Bordeaux
Bordeaux, 33000, France
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Centre Hospitalier Universitaire De Caen Normandie
Caen, France, 14033, France
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Centre Hospitalier Universitaire d'Angers
Angers, 49100, France
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Centre Hospitalier Universitaire de Clermont-Ferrand - Hôpital Gabriel Montpied
Clermont-Ferrand, 63003, France
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Centre Hospitalier Universitaire de Lille
Lille, 59037, France
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Centre Hospitalier Universitaire de Montpellier
Montpellier, 34295, France
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Centre Hospitalier Universitaire de Nantes - Hôpital Nord Laennec
Nantes, 44093, France
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Centre Hospitalier Universitaire de Nice
Nice, 06000, France
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Centre Hospitalier Universitaire de Rennes
Rennes, 35000, France
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Hôpital La Timone - APHM
Marseille, France, 13005, France
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Hôpital de la Pitié Salpêtrière
Paris, 75013, France
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Other studies related to the condition(s) this trial covers.
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