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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT03489278 Recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Clinical Procedures to Support Research in ALS

CAPTURE-ALS
Start date: February 15, 2018
Phase:
Study type: Observational

The purpose of the Clinical Procedures To Support Research (CAPTURE) study is to utilize information collected in the medical record to learn more about a disease called amyotrophic lateral sclerosis (ALS) and related disorders.

NCT ID: NCT03489200 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

EH301 for the Treatment of ALS

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

The objective of this trial is to evaluate the efficacy and tolerability of EH301 in patients with amyotrophic lateral sclerosis. Patients with ALS are randomized to receive either EH301 or placebo daily and undergo active evaluation for 6 months.

NCT ID: NCT03488524 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Open Label Extension Study of AMX0035 in Patients With ALS

CENTAUR-OLE
Start date: March 29, 2018
Phase: Phase 2
Study type: Interventional

This study will provide extended access to patients and assess longer-term outcomes on patients who have completed the Centaur study.

NCT ID: NCT03487263 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Dose-Escalation, Safety and Pharmacokinetic Study of IC14 in Motor Neurone Disease

Start date: October 1, 2017
Phase: Phase 1
Study type: Interventional

Ten patients with motor neurone disease (MND, also known as amyotrophic lateral sclerosis or ALS) will be successively enrolled to one of two dose levels of IC14 (human chimeric monoclonal anti-CD14) intravenously for four doses. Patients must be within 3 years of MND diagnosis and have adequate respiratory function. Safety, tolerability, immunogenicity, and PK/PD will be measured. To evaluate feasibility of the endpoints, additional endpoints of ALSFRS-R, respiratory function tests, disease biomarkers and patient-reported outcomes will be measured.

NCT ID: NCT03482050 Completed - Clinical trials for ALS (Amyotrophic Lateral Sclerosis)

A Study to Evaluate Transplantation of Astrocytes Derived From Human Embryonic Stem Cells, in Patients With Amyotrophic Lateral Sclerosis (ALS)

Start date: April 12, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This is a study of transplantation of Astrocytes derived from human embryonic stem cells, in patients with Amyotrophic Lateral Sclerosis (ALS). There will be no change in the routine ALS treatment of the patients enrolled into the study. Treatment will be administered in addition to the appropriate standard of care treatment. The study hypothesis is that transplantation of Astrocyte(AstroRx) cells can compensate for the malfunctioning of patients' own astrocytes by restoring physiological capabilities like the reuptake of excessive glutamate, reducing oxidative stress, reducing other toxic compounds, as well as by secreting different neuroprotective factors

NCT ID: NCT03481348 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Pharyngeal Electrical Stimulation in Amyotrophic Lateral Sclerosis

Start date: February 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

During the course of ALS most patients develop swallowing deficits. In this pilot study we investigate if dysphagia in ALS can be improved by Pharyngeal Electrical Stimulation (PES). PES is Communauté Européenne (CE-) certificated and has been approved for treatment of neurological, oropharyngeal dysphagia. During PES, electrical stimuli are applied at the pharynx via a nasogastral tube with the aim of triggering reorganization processes in damaged brain structures. There is evidence of a positive effect of PES in Stroke and Multiple Sclerosis patients.

NCT ID: NCT03474263 Withdrawn - Clinical trials for Amyotrophic Lateral Sclerosis

IC14 for Rapidly Progressive Amyotrophic Lateral Sclerosis (ALS)

Start date: September 1, 2019
Phase: Phase 2
Study type: Interventional

Patients with rapidly progressive ALS will be assigned to IC14 intravenously on Day 1-4. This 4-day course will be repeated on Days 8-11. Patients will all undergo MR-PET scans at two time points: before treatment onset and after the last treatment cycle. This scan will measure areas of ALS disease activity and assess response to IC14 treatment. MR-PET scans will be compared to historical controls.

NCT ID: NCT03472950 Recruiting - ALS Clinical Trials

Safety and Efficacy of Ranolazine for the Treatment of Amyotrophic Lateral Sclerosis

Start date: June 11, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to evaluate the safety and effectiveness of Ranolazine, and how well it is tolerated in patients with Amyotrophic Lateral Sclerosis (ALS). Ranolazine is an FDA approved drug that is used for decreasing chest pain.

NCT ID: NCT03464903 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Study of ALS Reversals 2: Genetic Analyses

StAR2
Start date: June 22, 2018
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to try to understand why reversals of amyotrophic lateral sclerosis (ALS) and primary muscular atrophy (PMA) take place. The study will enroll patients with ALS or PMA reversals to give saliva samples in order to determine if the ALS or PMA reversal is because of certain changes in the genetic code.

NCT ID: NCT03457753 Withdrawn - ALS Clinical Trials

Riluzole Oral Soluble Film Safety and Tolerability in Amyotrophic Lateral Sclerosis

Start date: March 1, 2018
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the safety and tolerability, with emphasis on the oral cavity, of ROSF (containing riluzole 50mg) in subjects with amyotrophic lateral sclerosis (ALS) administered twice daily for 12 weeks. Secondary objectives include (1) to record the subject's assessment of any difficulty taking riluzole administered as ROSF and any difficulty taking riluzole in the tablet formulation and (2) to record the relative preference, if any, of subjects and caretakers, for riluzole administered as ROSF vs. the riluzole tablet.