Condition
Amyotrophic Lateral Sclerosis clinical trials and research
As of November 12, 2026, Find a Trial lists 95 Amyotrophic Lateral Sclerosis clinical trials that are recruiting, at sites in 30 countries (most in United States (45), France (14), Italy (13)). 2 were first registered in the last 30 days. By phase: Phase 1/2 (7), Phase 1 (6), Phase 2 (3), Phase 2/3 (2). The most active sponsors are Istituto Auxologico Italiano (4), Mayo Clinic (3), Assistance Publique - Hôpitaux de Paris (3). There are also 65 NIH-funded research projects on Amyotrophic Lateral Sclerosis, with $136.4 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 95Clinical trials
- 65NIH research projects
- 2New in 30 days
- 30Countries
Newest Amyotrophic Lateral Sclerosis clinical trials
| Study | Phase | Where | Status | Registered |
|---|---|---|---|---|
| Implanted Brain-Computer Interface to Help People with Severe Arm Impairment | — | Miami, Florida | Recruiting | Nov 10, 2026 |
| Brain-computer interface chat tool for people with ALS | — | Santa Barbara, California | Recruiting | Oct 13, 2026 |
| BIIB147 safety and how it behaves in adults with ALS | Phase 1/2 | St Louis, Missouri and 1 other locations | Recruiting | Oct 2, 2026 |
| Aims to restore UNC13A function in people with ALS | Phase 1/2 | Lübeck, Schleswig-Holstein and 5 other locations | Recruiting | Jun 29, 2026 |
| LTX-002 in adults with ALS | Phase 1/2 | Lübeck and 4 other locations | Recruiting | Jun 22, 2026 |
| Repeated ultrasound-assisted blood-brain barrier opening in ALS | Phase 1/2 | Paris | Recruiting | May 6, 2026 |
| ALS master protocol with LY4256984 in eligible completers | Phase 1 | Leuven and 10 other locations | Recruiting | May 6, 2026 |
| Long-term safety test of LY4256984 in ALS patients | Phase 1 | Leuven and 10 other locations | Recruiting | May 6, 2026 |
| Using SleepImage to detect respiratory failure in people with ALS | — | London | Recruiting | Mar 31, 2026 |
| How physical functioning relates to quality of life for people with ALS at TidalHealth | — | Salisbury, Maryland | Recruiting | Mar 24, 2026 |
All recruiting trials (95)
-
Implanted Brain-Computer Interface to Help People with Severe Arm Impairment
We’re testing the N1 System, a fully implanted brain interface in the motor cortex with a robot, to see if it can help adults with spinal cord injury, ALS, or chronic stroke use a computer or keyboard more easily.
-
Brain-computer interface chat tool for people with ALS
This test compares a wearable brain-computer interface communication device to eye-tracking devices that people with ALS currently use to help them communicate.
-
BIIB147 safety and how it behaves in adults with ALS
This study tests BIIB147 in adults with ALS to see if it is safe and how the body handles it, including early and long-term effects.
-
Aims to restore UNC13A function in people with ALS
This trial tests TRCN-1023 in adults with ALS to see if it’s safe, tolerated, and shows early signs of benefit.
-
LTX-002 in adults with ALS
A study will test whether the experimental drug LTX-002 is safe and tolerable in adults with ALS and see how the body handles the drug and how it affects ALS indicators.
-
Repeated ultrasound-assisted blood-brain barrier opening in ALS
This trial tests whether repeatedly opening the blood-brain barrier with ultrasound is safe and may help people with ALS.
-
ALS master protocol with LY4256984 in eligible completers
This study tests LY4256984 in people with ALS who completed a parent ALS study, to see if it is safe and tolerable over about 96 weeks.
-
Long-term safety test of LY4256984 in ALS patients
This long-term extension study will see if LY4256984 is safe and tolerable in people with ALS who completed the earlier trial.
-
Using SleepImage to detect respiratory failure in people with ALS
This project will try SleepImage monitoring during an overnight sleep recording to see if it can detect early respiratory failure in adults with ALS.
-
How physical functioning relates to quality of life for people with ALS at TidalHealth
This study will see if physical functioning scores relate to quality of life for adults with ALS who receive care at TidalHealth Peninsula Regional.
-
EH-301 and N-acetylcysteine with Riluzole for early ALS
This will test whether adding EH-301 plus N-acetylcysteine to standard Riluzole can slow down or improve symptoms in people with ALS.
-
Connexus® Brain-Computer Interface to restore communication and device control
This study will try the Connexus brain-computer interface to help people with severe loss of voluntary movement (for example from ALS, cervical spinal cord injury, or stroke) communicate and control computers.
-
Personalized physiotherapy using robotic leg-press guidance for people with ALS
This study will try a personalized physiotherapy program guided by a robotic leg-press to see if it helps adults with ALS maintain physical function better than standard physiotherapy.
-
Blood RNA biomarkers for ALS using neuron-derived extracellular vesicles
This will try to see if RNA signatures in neuron-derived extracellular vesicles from blood can identify biomarkers in adults with suspected sporadic ALS compared with healthy volunteers.
-
Pridopidine for adults with early, rapidly progressing ALS
This trial will see if taking pridopidine 45 mg twice daily can slow disease progression in adults with early, rapidly progressing ALS.
-
Longitudinal integrated biomarker profiling linked to ALS clinical features
This project will test whether repeated blood and spinal-fluid biomarker measurements combined with deep clinical profiling can help predict disease course in adults with ALS.
-
Needs of adults with the C9orf72 form of ALS and their caregivers
This online survey will try to describe care and quality-of-life needs for adults with ALS who have the C9orf72 mutation and for their caregivers in Italy.
-
Video-based proprioceptive home exercise for trunk and limb control in ALS
This program will try a video-based proprioceptive home exercise routine for adults with ALS who can sit independently to see if it improves trunk and limb control and daily activities.
-
Single intrathecal injection of INS1202 for adults with ALS (SOD1 or no known mutation)
This study will try a single injection of INS1202 into the spinal fluid to see if it is safe and how it acts in adults with ALS who have SOD1 mutations or no known ALS gene mutation.
-
Safety and tolerability of VTx-002 given into the cisterna in people with ALS
This trial will test a single intracisternal injection of VTx-002 to see if it is safe and tolerated in adults with ALS.
-
Long-term safety monitoring of tofersen (Qalsody) in people with SOD1 ALS
This project will see how safe tofersen (Qalsody) is over time in people with ALS caused by SOD1 mutations by collecting health information without changing their care.
-
Terazosin and ATP in ALS: see if this drug helps energy in ALS patients
This pilot study tests whether terazosin, taken daily, can raise ATP levels and be safe for adults with ALS.
-
Robotic implantation of a precise brain‑computer interface to restore communication
This project tests whether a robotically implanted Neuralink N1 brain implant can help adults with severe, irreversible speech loss from ALS, spinal cord injury, or stroke communicate again.
-
Safety, tolerability, and how Amisodin is processed in healthy adults
Try whether single and short daily oral doses of Amisodin are safe and how the body handles the drug in healthy adults aged 18–55.
-
Acamprosate for ALS with C9orf72 mutation
This study tests whether acamprosate can be safely used to see if it helps people with ALS who carry a C9orf72 mutation.
-
Observational study on amyotrophic lateral sclerosis
This study is collecting health information from people with ALS, those with related genetic mutations, and healthy volunteers to help improve treatments and understand the disease better.
-
High-tech rehabilitation program for adults with chronic neuromuscular diseases
This trial will test whether a high-tech rehab program using robotic systems, virtual reality, and balance platforms works as well as traditional rehab to reduce fatigue and improve function in adults with chronic neuromuscular diseases.
-
Wireless brain implant for controlling devices
This study is testing a new wireless brain implant that helps paralyzed and amputee patients control devices just by thinking, to see if it can improve their daily lives.
-
How interactive tasks change how people hear speech from people with ALS.
We will test whether people without speech disorders hear speech from people with ALS differently when the speech comes from interactive versus non-interactive tasks.
-
Using digital technologies to measure physical impairments in ALS
This study is testing new digital tools to see how well they can measure physical challenges in people with ALS, making it easier for patients to participate without having to travel much.
-
Multicenter study using MRI to identify biomarkers in ALS patients
This study is trying to see if brain scans and blood tests can help track how ALS changes over time in patients compared to healthy people.
-
Treatment of Amyotrophic Lateral Sclerosis with TP04HN106
This study is testing a new drug called TP04HN106 to see if it can help people with ALS feel better and improve their condition.
-
Validation of the Polish Fatigue Severity Scale
This study is testing a Polish version of a questionnaire to see how well it measures fatigue in people with multiple sclerosis, ALS, and stroke.
-
Psilocybin therapy for patients with ALS and depression
This study is testing if psilocybin therapy can help people with ALS who are also feeling depressed.
-
Impact of Oral Nutrition Before Gtube Feeding in ALS Patients
This study is testing if eating a special nutrition formula before getting a feeding tube helps people with ALS handle the tube feedings better and possibly slow down their disease.
-
Collecting data on neurodegenerative diseases progression markers
This study is trying to find new signs that can help doctors understand how neurodegenerative diseases like Parkinson's progress, so they can improve early treatment options for patients.
-
Collecting data and samples from ALS patients and controls
This study is collecting health information and samples from people with ALS, those who carry ALS-related genes, and healthy individuals to help future research on ALS and similar conditions.
-
Evaluating RAG-17 for ALS patients with SOD1 mutation
This study is testing a new drug called RAG-17 to see if it is safe and effective for people with ALS who have a specific SOD1 gene mutation.
-
Comparing protein patterns in skin biopsies of neurodegenerative diseases
This study is trying to see if the patterns of certain proteins in skin samples can help doctors better understand and diagnose different neurodegenerative diseases like Alzheimer's, Parkinson's, and frontotemporal dementia.
-
Evaluating ranolazine for treating ALS symptoms
This study is testing if the medication ranolazine can help improve muscle cramps and quality of life for people with ALS.
-
Using Electrical Impedance Myography to Track ALS Progression
This study is testing if a new method using Electrical Impedance Myography can help track how ALS progresses in patients to improve future treatments.
-
Using skin cells to model ALS
This project will test whether skin cells taken by biopsy from people with ALS, people who carry ALS gene mutations but have no symptoms, and healthy volunteers can be used to model ALS in the lab.
-
Robotically implanted brain-computer interface for patients with severe paralysis
This study is testing a new brain implant that uses a robot to help people with severe paralysis communicate and control devices better.
-
Exploring brain connectivity in ALS and emotional symptoms
This study is testing how brain connections in people with ALS relate to emotional symptoms like sudden laughter or crying to better understand what's happening in their brains.
-
Neural stem cell treatment for ALS
This study is testing whether a new treatment using human neural stem cells can help people with ALS feel better and stay safe compared to a placebo.
-
Understanding the variability in ALS through biomarkers
This study is trying to see how different biological markers can help us understand the varying symptoms of ALS in patients and group them based on their unique characteristics.
-
Creating a database to study variations in motor neuron diseases
This study is trying to learn more about the different types of motor neuron diseases in patients to better understand the condition and improve how we predict its course.
-
Using the Quadriceps Combined Test to Diagnose and Monitor ALS
This study is testing a new way to diagnose and track ALS using a special test to see how well the muscles and nerves are working in people who might have the disease.
-
Evaluating how communication affects speech in people with ALS
This study is testing how different ways of talking affect speech in people with ALS compared to others their age.
-
Assessing the safety and effects of Darifenacin in ALS patients
This study is testing whether the medication Darifenacin is safe and can help people with ALS by looking at its effects on muscle function.
-
Monitoring movement in patients with ALS using a wearable device
This study is testing a new wearable device to see how daily movement patterns change in people with ALS over a year.
-
Understanding neuromuscular connections in ALS patients
This study looks at how the connections between nerves and muscles change in people with ALS to see if there are differences compared to healthy individuals and those with other diseases.
-
Biobank for studying ALS and Alzheimer's diseases
This study is collecting blood, skin samples, and health information from people to see how genetics might help us understand and find treatments for ALS and Alzheimer's disease.
-
Improving hand strength and function in ALS patients using brain and spinal cord stimulation
This study is testing a new way to help people with ALS improve their hand strength and function by using brain and spinal cord stimulation along with exercises.
-
Identifying factors related to weight loss in ALS patients
This study is trying to find out what causes weight loss in people with ALS by looking at their blood samples and health information to help improve their care.
-
Acetyl-L-carnitine to slow functional decline in ALS
This trial tests whether two doses of acetyl-L-carnitine can slow loss of independence in adults with recent-onset ALS.
-
Using a brain-computer interface to help people with speech difficulties communicate
This study is testing a brain-computer interface to help people who can't speak due to conditions like ALS communicate by turning their thoughts into speech.
-
Targeted RNA sequencing for diagnosing ALS
This study is testing a new way to use RNA sequencing to help diagnose ALS more accurately by looking for specific genetic changes in people who have been prescribed genetic testing for the disease.
-
Using virtual reality to ease breathing difficulties in ALS patients on ventilation
This study is testing if virtual reality can help ease breathing difficulties for ALS patients who use a ventilator.
-
Accelerated repetitive transcranial magnetic stimulation for ALS
This study is testing a new type of brain stimulation to see if it can help people with ALS feel better and improve their muscle strength over 24 weeks.
-
Evaluating a device to improve breathing in ALS patients
This study is testing a breathing device to see if it can help people with ALS improve their cough and breathing over four weeks.
-
Evaluating the Nervous System in ALS Patients
This study is testing if skin samples can help track how the nervous system is affected in people with ALS over 18 months after their symptoms start.
-
Impact of long-term ventilation support on ALS patients and their families
This study is testing how long-term breathing support affects the quality of life for people with ALS and their families.
-
Using a neural interface to help people with tetraplegia control devices with their thoughts
This study is testing a new brain interface that helps people with tetraplegia, especially those with ALS, control devices like computers just by thinking about it.
-
Understanding the burden on ALS patients and their caregivers
This study looks at the emotional struggles faced by people with ALS and their caregivers to see how they feel about being a burden and the stress that comes with it.
-
Collecting data and samples from ALS patients and their families
This study is collecting blood samples and health information from people with ALS and their families to help researchers learn more about the genetic causes of the disease.
-
Collection of biological samples for diagnosing rare neurological diseases
This study is collecting blood and spinal fluid samples from people with rare neurological diseases to see if they can find new markers that help diagnose these conditions more accurately.
-
Using diaphragmatic ultrasound to monitor breathing function in ALS patients
This study is testing how ultrasound can help track breathing problems in people with ALS before they need breathing support.
-
Monitoring swallowing function and quality of life in ALS patients
This study looks at how swallowing problems affect the quality of life for people with ALS and how they feel about getting a feeding tube.
-
Platform to analyze and understand ALS
This study is trying to gather and analyze a lot of information about ALS and related disorders by having participants, including healthy individuals, come in for check-ups and tests over a year to help improve future research.
-
Creating a biorepository of biofluids and clinical data for ALS research
This study is collecting blood, spinal fluid, and urine samples from people with ALS and healthy individuals to help find new ways to understand and treat the disease.
-
Exploring genetic causes of ALS in Norway
This study is trying to find out if certain genes are linked to ALS by asking people with the disease in Norway about their family history and taking a blood sample for testing.
-
Collecting blood and CSF samples to study ALS and related disorders
This study is collecting blood and spinal fluid samples from people with ALS and similar disorders to see if they can find helpful markers for diagnosing and tracking the disease.
-
Using muscle activity measurements to improve ALS diagnosis
This study is testing if a new way of measuring muscle activity can help doctors diagnose ALS more accurately and track how the disease changes over time.
-
Analysis of ALS patient tissues and registry
This study is trying to gather information from people with ALS to better understand the disease and find new ways to treat it.
-
Registry of ALS patients receiving Traditional Chinese Medicine
This study is creating a registry to track ALS patients who are using traditional Chinese medicine to see how it affects their health over five years.
-
Measuring daily activity in patients with ALS and healthy controls
This study is testing how active people with ALS are compared to healthy individuals by using a special device to track their daily movements over a year.
-
Analyzing macrophages in ALS and related motor impairments
This study is trying to see if looking at certain immune cells in people with ALS and related motor issues can help find new ways to treat the disease.
-
Understanding the natural history and clinical features of ALS in China
This study looks at how Amyotrophic Lateral Sclerosis (ALS) affects people in different parts of China and how the disease has changed over time to help improve diagnosis and treatment.
-
Longitudinal study of frontotemporal lobar degeneration
This study is trying to learn more about frontotemporal lobar degeneration by following both affected individuals and their family members over time to see how the condition develops.
-
RAPA-501 therapy for ALS
This study is testing a new treatment called RAPA-501 to see if it can help slow down the progression of ALS in patients.
-
Understanding how Edaravone works in different types of ALS patients
This study is trying to see how the medication Edaravone affects different types of ALS patients and which ones might benefit the most from it.
-
Observing the natural history of amyotrophic lateral sclerosis in patients
This study is looking at how amyotrophic lateral sclerosis (ALS) progresses in Chinese patients to better understand the disease and find out what might affect its course.
-
Investigation of a brain-computer interface system for communication in patients with severe disabilities
This study is testing a new brain-computer interface that helps people with severe disabilities, like tetraplegia and ALS, communicate better by using signals from their brain.
-
Research to gather clinical data on ALS and related disorders
This study is collecting health information from people with ALS and similar disorders to better understand these conditions and help improve future treatments.
-
Understanding neurodegenerative disorders like ALS and frontotemporal dementia
This study is trying to see if adults with neurodegenerative disorders like ALS and frontotemporal dementia can join future research by checking their health and collecting samples for further testing.
-
Identifying biomarkers of synaptic damage in multiple sclerosis
This study is testing blood and spinal fluid samples from people with multiple sclerosis to see if certain markers can help us understand brain changes and how the disease progresses.
-
Masitinib added to riluzole versus placebo for people with ALS
This trial tests whether adding masitinib to standard riluzole treatment slows disease progression in people with ALS.
-
Treatment for neurologic disorders using stem cells
This study is testing whether using stem cells from patients' own bone marrow can help improve brain and nerve function in people with serious neurologic disorders that don't respond well to regular treatments.
-
MRI markers for ALS and PLS
The study will use 3T and 7T MRI scans to see if specific brain imaging markers differ between people with ALS or PLS and healthy volunteers.
-
Registry for understanding Amyotrophic Lateral Sclerosis in the U.S.
This study is collecting information about ALS in the U.S. to see how common it is and what factors might be linked to the disease.
-
Feasibility of a brain-computer interface for people with tetraplegia
This study is testing a new brain-computer interface that helps people with tetraplegia control a computer and other devices just by thinking, to see if it’s safe and effective.
-
Creating stem cells from existing human cells to study ALS
This study is trying to create special stem cells from regular human cells to better understand ALS and find new treatments for it.
-
Study of healthy individuals at genetic risk for ALS
This study is looking at healthy people who have a family history of ALS to see how their genes and environment might affect their chances of developing the disease in the future.
-
Research on Amyotrophic Lateral Sclerosis and related conditions
This study is trying to understand how ALS relates to other nerve diseases and to find new ways to track its progress by looking at people with ALS, those at risk, and healthy individuals.
NIH-funded research (newest 40 of 65)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
-
Investigating how DNA damage and repair mechanisms are altered in ALS and frontotemporal dementia.
This study is looking at how problems with DNA repair might contribute to conditions like ALS and frontotemporal dementia, and it’s testing ways to fix these issues in cells from patients to help develop new treatments.
-
Understanding how work exposures and genes influence ALS risk
A study is building a long-term group of people at higher risk for ALS to see how their jobs, exposures at work, and genes together affect if and when the disease might develop.
-
NUZ-001: a treatment option for ALS to protect nerve cells
A small molecule called NUZ-001 is being tested to help people with ALS by improving cell systems that keep proteins balanced and prevent harmful protein clumps.
-
Alpha5 integrin's role in ALS: how a cell switch worsens disease
Aims to understand how a specific protein called alpha5 integrin in immune cells affects ALS progression and whether blocking it can help extend life.
-
C9orf72 ALS/FTD Prevent: prepping for future treatment
This grant aims to get ready for a preventive treatment for people who carry the C9orf72 genetic change that can lead to ALS or frontotemporal dementia.
-
Air pollutants and ALS: mapping environmental links to motor neuron disease
This NIH grant explores whether different air pollutants are linked to the development of ALS and uses a large U.S. data set to look for environmental risk factors.
-
CNM-Au8 Expanded Access for ALS patients across the U.S.
A wide-access program is testing CNM-Au8, a neuroprotective medicine, for people with ALS across all 50 states.
-
Access to CNM-Au8 for people with ALS
This program offers people with ALS access to CNM-Au8, an experimental oral therapy that aims to protect motor neurons and support cellular energy.
-
How a tiny virus carrier could protect nerve cells in ALS Veterans
Researchers are testing a new gene-delivery approach to help protect nerve cells and improve function for people with ALS, with a focus on Veterans.
-
Digital speech markers to track bulbar decline in Spanish-speaking ALS patients
A smartphone app will collect Spanish-language speech data from ALS patients to detect early bulbar decline and help guide timely care.
-
Pridopidine for ALS: Expanded Access Protocol for S1R-targeted Therapy
This project tests pridopidine, a Sigma-1 receptor drug, for people with ALS to see if it can help symptoms or slow progression.
-
Understanding how a genetic repeat causes harmful protein production in ALS/FTD
Aimed at uncovering how a genetic repeat in the C9orf72 gene triggers abnormal protein production that damages nerve cells in ALS and FTD.
-
Personalized anti-inflammatory T cell therapy for ALS
This program offers a treatment using your own modified immune cells (RAPA-501) to reduce nerve inflammation for people with ALS who have low lung capacity.
-
HERV-K Immunization Strategy to Help ALS Hold the Line Against Progression
A new immunotherapy approach aims to help people with ALS by targeting a virus-related protein believed to contribute to nerve cell damage.
-
AAV-CRISPR therapy for a genetic cause of ALS/FTD
A team is testing a gene-editing approach to potentially treat a genetic form of ALS and a related dementia by targeting the C9orf72 gene with a precise CRISPR method.
-
Enhancing rehabilitation for people with ALS using breathing-friendly training
Aims to boost how well people with ALS recover and maintain movement and breathing by pairing traditional rehabilitation with a special pre-treatment called therapeutic acute intermittent hypoxia.
-
Identifying how neurofilament regulation and turnover work in ALS
AIMS to understand how neurofilaments behave in ALS to improve biomarkers and treatment strategies for people with ALS.
-
TDP43 breakdown in ALS: how brain cells use lysosomes to clear trouble
This grant supports a clinician-scientist at UCSF as they study how the protein TDP-43 is removed by lysosomal enzymes to protect nerve cells in ALS.
-
Nucleolus dysfunction and ALS: understanding motor neuron disease at the cellular level
Aims to understand how problems in the neuron’s nucleolus contribute to ALS and how key proteins behave in models to guide future therapies for people with ALS.
-
Biomarker test for early ALS diagnosis using Nano-QuIC detection of misfolded TDP-43
A new blood, spinal fluid, or nasal swab test using Nano-QuIC aims to detect misfolded TDP-43 early in people at risk for ALS to speed up diagnosis and treatment.
-
Social connectedness in ALS patients and how speech impairments affect it
A large study with ALS patients will track how speech and mobility difficulties influence social connections using smartphones over six months.
-
Multi-Target RNA Therapies for ALS and Alzheimer's Disease
A patient-friendly look at a project that aims to develop RNA-based medicines to slow or modify ALS and Alzheimer’s-related diseases by targeting multiple genes.
-
Spinal and brain stimulation to boost hand and arm movement in ALS
This project pairs mild spinal-cord and brain stimulation to help people with ALS strengthen hand and arm movements.
-
How chemically damaged RNA might drive ALS
Researchers will look at whether chemically damaged RNA in nerve cells causes motor neuron loss and speeds up ALS.
-
How C9orf72 RNA repeats make toxic proteins in ALS and FTD
This research looks for how a repeated RNA sequence in the C9orf72 gene creates toxic proteins that can harm people with ALS or FTD.
-
Speeding up gene‑editing to target the C9ORF72 form of ALS
This project builds faster, more precise gene‑editing tools aimed at removing the harmful C9ORF72 repeat mutation in adults with ALS.
-
Expanded access to pridopidine for people with ALS
This program offers people living with ALS access to the experimental drug pridopidine while collecting information about safety and how it affects symptoms.
-
RAPA-501 immune-cell therapy for ALS (expanded access for advanced disease)
This program offers an experimental immune-cell treatment called RAPA-501 to people with ALS who have advanced breathing weakness (SVC <50%).
-
Engineered regulatory immune cells to protect nerves in ALS
Engineered regulatory immune cells (CAR Tregs) that seek out misfolded SOD1 and calm inflammation around motor neurons in people with ALS.
-
Understanding how nerve cell proteins change in ALS
This project aims to understand how certain proteins in nerve cells, called neurofilaments, are regulated and cleared in people with ALS.
-
Understanding how RNA oxidation affects the onset and progression of ALS
This study is looking at how damaged RNA might play a role in the development of ALS, focusing on how it affects the health of motor neurons, and it's designed for people interested in understanding more about the disease and its progression.
-
Understanding Social Connections for People with ALS
This project looks at how speech and movement challenges affect social connections for people with ALS, aiming to find ways to help them stay connected.
-
Cell and tissue changes that lead to sporadic ALS and frontotemporal dementia
This project looks at how physical changes inside cells and in their tissue can make TDP‑43 protein clump in people with sporadic ALS and frontotemporal dementia.
-
Gene Therapy for ALS
This project is exploring a new gene therapy delivered to the spine to help stop or slow down Amyotrophic Lateral Sclerosis (ALS) in its early stages.
-
Using engineered immune cells to treat ALS
This study is exploring a new way to help people with ALS by using specially designed immune cells to target harmful proteins in the body, with the hope of reducing inflammation and slowing down the disease.
-
Understanding ALS Risk in Workers with Certain Occupations
This project is creating a group of people at higher risk for ALS to learn how their jobs and genes might lead to the disease.
-
Developing new therapies for ALS and related neurodegenerative diseases
This study is looking for new ways to treat neurodegenerative diseases like ALS and Alzheimer's by using special medicines that target specific genes, and it invites patients to join trials to explore these exciting new options.
-
Investigating new treatments for frontotemporal dementia and ALS using gene editing
This study is looking at ways to help people with frontotemporal dementia and ALS by using a special gene-editing tool to fix a harmful gene that causes these diseases.
-
Improving decision-making for swallowing difficulties in ALS patients
This study is all about helping people with ALS who have trouble swallowing by creating a helpful tool that guides them and their caregivers in making informed choices about feeding tubes, so they can feel more confident and satisfied with their decisions.
-
Understanding motor neuron damage in ALS patients
This study is looking into what causes damage to the nerves that control movement in people with ALS, using advanced imaging and brain analysis to better understand the connection between brain changes and the symptoms you experience, all with the goal of improving how we diagnose and understand the condition.
Related topics
Quick answers
How many Amyotrophic Lateral Sclerosis clinical trials are recruiting right now?
95, as of November 12, 2026. 2 of them were first registered in the last 30 days. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 30 countries. The most sites are in United States (45 trials), France (14 trials), Italy (13 trials), Canada (7 trials), Belgium (7 trials). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 1/2: 7, Phase 1: 6, Phase 2: 3, Phase 2/3: 2. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.