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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT03073239 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis: a New Paradigm

ALSParadigm
Start date: December 2016
Phase:
Study type: Observational

Amyotrophic Lateral Sclerosis (ALS) is a degenerative neuromuscular disease, progressing inexorably to respiratory failure, the by involvement of respiratory muscles, the commitment with most impact on the prognosis of ALS. According to current knowledge, the clinical presentation of the disease is characterized by spinal or bulbar involvement, the latter being associated with a worse prognosis. There are multiple factors described in the aetiology of ALS, as the successive damage the motor neuron, which can happen in high-impact athletes, or exposure to heavy metals. Genetic mutations are also described, being associated to a higher prevalence of ALS. Data from retrospective studies with ALS populations reveal a prevalence of 4-8 cases per 100,000 persons. Research carried out in Trás-os-Montes e Alto Douro region (Northeast of Portugal) shows a high prevalence of ALS, with near 10 cases per 100,000 persons, with a recent increase in the bulbar involvement. The reasons for the high prevalence of ALS in this region are unknown.

NCT ID: NCT03068754 Terminated - Clinical trials for Amyotrophic Lateral Sclerosis

Study of Acthar® Gel (Acthar) for Amyotrophic Lateral Sclerosis (ALS)

Start date: June 22, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

About 213 people with ALS will participate in this study. There will be locations in North and South America. During the first part, participants will be randomly assigned to a group (like by flipping a coin). Out of every 3: - 2 will get the study drug - 1 will get a look-alike with no drug in it (placebo) During the second part, everyone will get the study drug. Participation will help doctors find out if Acthar can help or slow down the symptoms of ALS better than placebo.

NCT ID: NCT03067857 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Autologous Bone Marrow-Derived Stem Cell Therapy for Motor Neuron Disease

Start date: September 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Herein, the investigators study the safety and efficacy of transplanting purified autologous bone marrow-derived stem cells transplanted via the intrathecal route by interventional radiology and the intravenous route.

NCT ID: NCT03049046 Recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

CC100: Phase 1 Multiple-Dose Safety and Tolerability in Subjects With ALS

CC100B
Start date: April 7, 2017
Phase: Phase 1
Study type: Interventional

Approximately 21 subjects with amyotrophic lateral sclerosis (ALS) will be randomized (6 to 1) to receive by mouth seven morning doses of CC100 or placebo for 7 days. Subjects are required to stay in the Clinic for approximately 9 hours following the first and last dose. Subjects will also have a mid-week clinic visit and will be contacted by phone within 3 to 5 days after the last dose. Funding Source - FDA OOPD

NCT ID: NCT03039673 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

MIROCALS: Modifying Immune Response and OutComes in ALS

MIROCALS
Start date: June 19, 2017
Phase: Phase 2
Study type: Interventional

MIROCALS is a phase II study of ld-IL-2 as a therapeutic agent for ALS. A randomized (1:1), placebo-controlled, double-blind, parallel group trial will be carried out to assess ld-IL-2 safety and clinical efficacy on survival and functional decline in newly diagnosed ALS patients treated for 18 months. Randomization will be stratified according to (i) country (n = 2 levels: UK, France) and (ii) site of onset (n= 2 levels: bulbar vs limb onset). The primary objective to evaluate the clinical efficacy and safety of the experimental drug (ld IL-2) over an 18 months period in order to establish the proof of concept (PoC) that modifying immune responses through the enhancement of regulatory T cells modifies the rate of ALS disease progression.

NCT ID: NCT03034317 Withdrawn - Clinical trials for Amyotrophic Lateral Sclerosis

NeuRx Diaphram Pacing System (DPS) Use in Amyotrophic Lateral Sclerosis (ALS)

PARADIGM
Start date: February 2, 2017
Phase: N/A
Study type: Interventional

The purpose of this research study is to collect more information about the use, safety, and effectiveness of the NeuRx DPS® in ALS patients.

NCT ID: NCT03020797 Terminated - Clinical trials for Amyotrophic Lateral Sclerosis

A Clinical Trial to Evaluate the Safety and Efficacy of Fycompa in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Start date: January 12, 2017
Phase: N/A
Study type: Interventional

This is a pilot trial to test perampanel (Fycompa; Eisai, Inc.) in ALS patients. The investigators will focus on safety and preliminary signs of efficacy. Perampanel is approved by the FDA for treatment of seizures in patients with epilepsy. In this study, perampanel will be used off-label for adults with ALS at an oral medication dose on the low end of the recommended dose range for epilepsy. This study will consist of two treatments arms: perampanel and matching placebo randomized at a 1:1 ratio. Subjects will receive medication for 9 months.

NCT ID: NCT03019419 Completed - ALS Clinical Trials

Perampanel for Sporadic Amyotrophic Lateral Sclerosis (ALS)

Start date: April 24, 2017
Phase: Phase 2
Study type: Interventional

To investigate the safety and the efficacy of perampanel in patients with sporadic amyotrophic lateral sclerosis

NCT ID: NCT03016897 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

ALS Testing Through Home-based Outcome Measures

ALS AT HOME
Start date: February 22, 2017
Phase:
Study type: Observational

ALS AT HOME is a single-center study of up to 150 participants being done to determine the extent to which frequent sampling can improve the qualities of outcome measures collected at home by study participants.

NCT ID: NCT02988297 Not yet recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Nebulized RNS60 for the Treatment of Amyotrophic Lateral Sclerosis

Start date: October 2024
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether nebulized RNS60 is effective in the treatment of amyotrophic lateral sclerosis (ALS).