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NCT06365216Active, not recruitingPhase 2

ALS Phase II Study of NX210c

A Double-blind, Randomized, Placebo-controlled, Multicentric, Phase II Study in Adult Patients With Amyotrophic Lateral Sclerosis (ALS) to Assess Efficacy, Safety, Tolerability and Pharmacokinetics of Multiple Intravenous Infusions of NX210c

Source: ClinicalTrials.gov · Last updated 24 Dec 2025

Brief summary (registry, in English)

This study will investigate the efficacy, safety, tolerability and pharmacokinetics (PK) of multiple intravenous infusions of NX210c, at two dose levels, in patients with Amyotrophic lateral sclerosis (ALS).

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
First submitted
9 Apr 2024
Start date
25 Oct 2024
Primary completion date
1 Feb 2026
Lead sponsor
Axoltis Pharma
NCT number
NCT06365216
EU CT number
2023-508895-13-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 80
  • From 25 Oct 2024 to the primary completion date, 1 Feb 2026
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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.

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

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

SiteCityCountrySite status
Centre Hospitalier Universitaire D'Angers
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AngersFranceCompleted
Centre hospitalier Universitaire de Bordeaux
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BordeauxFranceCompleted
Centre Hospitalier Régional et Universitaire de Brest
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BrestFranceCompleted
Hospices Civils de Lyon
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BronFranceCompleted
Centre Hospitalier Universitaire De Caen Normandie
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Caen Cedex 9FranceCompleted
Centre Hospitalier Universitaire de Clermont-Ferrand - Hôpital Gabriel Montpied
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Clermont-Ferrand Cedex 1FranceCompleted
Centre Hospitalier Universitaire De Lille
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Lille CedexFranceCompleted
Centre Hospitalier Et Universitaire De Limoges
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Limoges Cedex 1FranceCompleted
Hôpital La Timone - APHM
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MarseilleFranceCompleted
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceCompleted
CHRU de Nancy
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NancyFranceCompleted
Centre Hospitalier Universitaire de Nantes - Hôpital Nord Laennec
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Nantes Cedex 01FranceCompleted
Centre Hospitalier Universitaire de Nice
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NiceFranceCompleted
Hôpital de la Pitié-Salpêtrière
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ParisFranceCompleted
Centre Hospitalier Universitaire de Rennes
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RennesFranceCompleted
Centre Hospitalier Regional Universitaire De Tours
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Tours Cedex 9FranceCompleted

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