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Amyotrophic Lateral Sclerosis clinical trials

View clinical trials related to Amyotrophic Lateral Sclerosis.

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NCT ID: NCT04960540 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Multimodal Brain Imaging Study

Start date: August 1, 2019
Phase:
Study type: Observational

To explain the key brain network nodes and their brain mechanisms of ALS language cognitive impairment and decline, reveal the neural mechanism of the association between ALS language cognitive impairment and motor executive function, and provide potential early diagnostic markers and targeted therapeutic targets for ALS language cognitive impairment.

NCT ID: NCT04948645 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

A Phase 1 Study to Investigate the Safety and Pharmacokinetics of ABBV-CLS-7262 in Patients With Amyotrophic Lateral Sclerosis

Start date: September 22, 2021
Phase: Phase 1
Study type: Interventional

ABBV-CLS-7262 is an investigational drug being researched for the treatment of Amyotrophic Lateral Sclerosis. This is an up to 156-week, 2-part study. Part 1 will be a 4-week, randomized, double-blind, placebo-controlled study; Part 2 will be up to a 152-week active treatment extension (ATE) during which all subjects will receive ABBV-CLS-7262.

NCT ID: NCT04866771 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Remotely Supervised tDCS for Slowing ALS Disease Progression

Start date: August 27, 2021
Phase: N/A
Study type: Interventional

Most ALS care is centered on patient support and symptom management, making rehabilitation an integral aspect for slowing disease progression, prolonging life span, and increasing quality of life. Brain stimulation has been increasingly explored as a promising neuromodulatory tool to prime motor function in several neurological disorders. We propose a novel mechanism using remotely supervised brain stimulation to preserve motor function in individuals with ALS. This project will also aim to explore the effectiveness of brain stimulation on upper and lower motor neuron mechanisms in individuals with ALS.

NCT ID: NCT04745299 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Evaluation the Efficacy and Safety of Mutiple Lenzumestrocel (Neuronata-R® Inj.) Treatment in Patients With ALS

ALSummit
Start date: March 23, 2021
Phase: Phase 3
Study type: Interventional

ALSUMMIT is a double-blind, randomized, placebo-controlled, multi-center, parallel, phase III clinical trial to evaluate and confirm the efficacy and long-term safety of repeated Lenzumestrocel (Neuronata-R® inj.) treatment.

NCT ID: NCT04651855 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

The Evaluation of the Effect of Mesenchymal Stem Cells on the Immune System of Patients With ALS

ALSTEM
Start date: December 2, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to evaluate the safety of intrathecal administration of Wharton's Jelly Mesenchymal Stem Cells (WJMSC) and the impact on the immune system of patients with Amyotrophic Lateral Sclerosis.

NCT ID: NCT04494256 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

A Study to Assess the Safety, Tolerability, and Effect on Disease Progression of BIIB105 in Participants With Amyotrophic Lateral Sclerosis (ALS) and Participants With the ALS Ataxin-2 (ATXN2) Genetic Mutation

ALSpire
Start date: September 28, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The ALSpire Study is a clinical trial evaluating the investigational drug BIIB105 in adults living with amyotrophic lateral sclerosis (ALS). The ALSpire Study consists of two parts: - Part 1: 6-month placebo-controlled study. During Part 1, participants are randomly assigned to receive either BIIB105 or placebo in a 3:1 or 2:1 ratio (depending on the participant's assigned Cohort). - Part 2: up to 3-year long-term open-label extension. During Part 2, all participants receive BIIB105. The objectives of the study are to evaluate: - The safety and tolerability of BIIB105 in people with ALS - What the body does to BIIB105 (also called "pharmacokinetics") - What BIIB105 does to the body (also called "pharmacodynamics") - Whether BIIB105 can slow the worsening of clinical function

NCT ID: NCT04297683 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

HEALEY ALS Platform Trial - Master Protocol

Start date: July 14, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

The HEALEY ALS Platform Trial is a perpetual multi-center, multi-regimen clinical trial evaluating the safety and efficacy of investigational products for the treatment of ALS.

NCT ID: NCT04259255 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Radicava® (Edaravone) Findings in Biomarkers From ALS (REFINE-ALS)

Start date: October 21, 2019
Phase:
Study type: Observational

REFINE-ALS is a prospective, observational, longitudinal, multicenter study designed to identify biomarkers to serve as quantifiable biological non-clinical measures of Edaravone effects in ALS. Epigenetic and protein biomarkers will also be investigated.

NCT ID: NCT04240925 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Tolerability, Safety and Efficacy of Sigh Breaths During NIMV in Motor Neuron Disease

Start date: May 25, 2018
Phase: N/A
Study type: Interventional

Non-invasive mechanical ventilation (NIMV) is the recommended standard of care as initial therapy for patients with motor neuron disease (MND) with deterioration of the respiratory function. SIGH_01 study is aimed at investigating the tolerability, safety profile and efficacy of sigh breaths during non-invasive mechanical ventilation in patients with MND in comparison to the standard ventilation support protocol.

NCT ID: NCT04220021 Active, not recruiting - Clinical trials for Frontotemporal Dementia

Safety and Therapeutic Potential of the FDA-approved Drug Metformin for C9orf72 ALS/FTD

Start date: January 10, 2020
Phase: Phase 2
Study type: Interventional

The primary objective is to assess the safety and tolerability of Metformin in subjects with C9orf72 amyotrophic lateral sclerosis administered for 24 weeks. The overall objective is to determine if Metformin is safe in C9orf72 ALS patients and is a potentially viable therapeutic treatment for C9-ALS that reduces repeat-associated non-canonical start codon - in DNA (non-ATG) (RAN) proteins that are produced by the C9orf72 repeat expansion mutation.