Intense research is being conducted in many areas related to ALS, from basic science seeking the roots of the disease, to therapy development to find effective treatments.
Research into familial (running in families) forms of the disease also may have relevance for sporadic (nonfamilial) forms, as all ALS cases — regardless of the form — present and develop along similar lines.
Many other medications and treatments are being tested for potential benefits in ALS. See Clinical Trials  for details.
This section offers an overview and links to more information about ALS research targets and strategies, and research administration in ALS.
While some research teams have focused their attention on microglia, the nervous system's immune cells, others have focused more on astrocytes, a type of glial cell that normally provides support to motor neurons and other cells in the nervous system. Among their roles is clearing away a potentially toxic compound called glutamate from the area around nerve cells.
In late 2008, investigators showed that treating astrocytes alone  can delay disease onset and extend survival in mice with a disease resembling ALS caused by mutations in the SOD1 gene.
In 2011, researchers showed that toxicity from astrocytes  causes nerve cells to degenerate in new models for both inherited and noninherited forms of ALS.
Study results from two experiments reported in 2013 showed that astrocyte-associated harm to motor neurons may differ  depending not only on whether the astrocytes carry a mutation, but on which mutation they carry as well.
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Many genes, when mutated, can cause familial ALS. Among them are the SOD1 gene, the TDP43 gene and the FUS gene . In 2011, researchers discovered that abnormalities in the ubiquilin 2 gene  can cause ALS, and a specific mutation in the C9ORF72 gene  was found to be the most common genetic cause of the disease identified so far. (See Causes/Inheritance .) If someone with an ALS-causing gene mutation is the first in the family to show the disease, the disorder is classified as sporadic, since there is no family history. (This can happen when, for example, a parent carrying the ALS-causing mutation passes away of other causes before ALS develops but not before passing the mutation along to his or her children.)
However, research on the genetic factors that contribute to ALS, without necessarily causing it directly, is of great interest. Scientists suspect that a number of gene variants — probably in combination with other unknown factors — may increase susceptibility to sporadic ALS.
Several large gene association studies have been done comparing the DNA of people with and without ALS in hopes of uncovering genetic differences. These studies have pointed toward potential genetic targets for ALS research. For example, a large, multinational study to identify genetic risk factors associated with ALS found two DNA sequences  on chromosomes 9 and one on chromosome 19 that are significantly different in people with and without the disease and may contribute to its development.
When scientists studied DNA from 915 people with ALS and 980 without the disease, they found expanded ataxin 2 genes in 43 (4.7 percent) of those with ALS and only 14 (1.4 percent) of those without it. They concluded that ataxin 2 expansions  are significantly correlated with increased risk for developing ALS. Expanded ataxin 2 protein molecules appear to have toxic interactions with TDP43, another protein implicated in ALS, and blocking ataxin 2 interactions with TDP43 could become a new therapeutic avenue.
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In ALS, there is some evidence that excess amounts of the neurotransmitter glutamate accumulate in the spaces around a nerve cell after it has completed its signaling function, causing problems for nerve cells the vicinity.
Normally, glutamate — a chemical transmitter of signals between nerve cells — is released by a sending neuron and docks on a receiving neuron. Once docked, it is quickly cleared away by glutamate transporter proteins, which are produced by neighboring cells in the nervous system called astrocytes. In ALS, something may go wrong with this glutamate clearance system. Some studies have suggested that, in ALS, a protein called EAAT2  may not be as efficient at clearing glutamate away from nerve cells as it should be. Other studies have suggested that a glutamate receptor, a docking site on the surface of motor neurons that receives glutamate, may be excessively permeable in this disease.
A drug specifically approved for the treatment of ALS by the U.S. Food and Drug Administration (FDA) is riluzole (Rilutek) , which is believed to interfere with the action of glutamate.
In 2011, MDA awarded a grant to the biotechnology company Glialogix  to test its new, experimental glutamate inhibitor called GLX1112  in mice with the SOD1-related familial form of ALS. The drug is designed to decrease excessive glutamate signaling through its interaction with a target on microglial cells, the immune cells of the nervous system.
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There is a growing body of evidence that malfunction of the immune system  is at least part of the ALS disease process. Researchers at the MDA-supported ALS Therapy Development Institute (ALS TDI)  and others have identified abnormal immune system overactivity in animal models of the disease, and the ALS TDI investigators have observed it in blood samples from people with ALS.
It had been thought that motor neurons died alone in ALS. But, today, there is evidence that immune system cells in the nervous system called microglia  are probably involved in their demise.
Blocking parts of the immune system  is a strategy being pursued by researchers at the ALS TDI. In 2011, this MDA-supported institute announced it would pursue testing in ALS mice of two experimental compounds that disrupt parts of the immune system. One, CDP7657 , is an antibody fragment that inhibits the immune response by targeting a protein called CD40L. The other, CTLA4-FC , targets a signaling protein called CD86.
In 2013, ALS TDI announced it it had received FDA approval to conduct a phase 2 trial of Gilenya (TDI 132, fingolimod) in ALS. Gilenya dampens the immune response and is approved by the FDA for the treatment of multiple sclerosis.
In addition, scientists at Neuraltus Pharmaceuticals  are working on an experimental drug called NP001 , which is designed to switch immune system cells from a damaging to a protective mode of action. In late 2010, Neuraltus announced encouraging findings  showing that NP001 was safe and well-tolerated at four different dose levels in people with ALS and that, after a single intravenous dose, there was an improvement in blood levels of a biomarker thought to be involved in ALS progression.
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Cellular proteins normally fold only in certain ways shortly after they're produced. When folding goes wrong, the result may be a highly toxic protein. In 2010, researchers found that misfolded SOD1 protein, unaccompanied by an SOD1 gene mutation, could underlie at least some cases of sporadic ALS .
Other proteins besides SOD1 may misfold and contribute to the disease as well. For example, the TDP43 and FUS proteins appear to misfold and form clumps  (aggregate) in ALS-affected motor neurons even when the genes for these proteins are normal.
Normally, proteins called chaperones help coax other proteins to fold into the correct shape. Therefore, some scientists are working on increasing levels of these chaperone proteins. An experimental drug called arimoclomol is being tried in SOD1-related familial ALS  with this mechanism in mind. A trial of arimoclomol in sporadic ALS also had been planned but did not go forward because of concerning data from toxicity studies in animals.
Another approach to targeting misfolded SOD1 is a type of molecule called an antisense oligonucleotide, which keeps toxic, misfolded SOD1 from being made. In 2012, the antisense-based drug ISIS-SOD1-Rx was found to be safe and well-tolerated  in people with SOD1-related familial ALS in a phase 1 clinical trial. The drug was developed by Isis Pharmaceuticals  with support from MDA.
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In ALS, the cellular "energy factories" called mitochondria malfunction, although it isn't clear exactly where in the chain of events of the ALS disease process this malfunction occurs.
When mitochondria malfunction, they may fail to produce the needed energy for cells, and they may leak toxic substances called reactive oxygen species, subjecting cells to a kind of poisoning known as oxidative stress .
Unfortunately, coenzyme Q10 , which combats oxidative stress, was not found to be helpful in people with ALS, even at high doses. (Coenzyme Q10 is an antioxidant, which is a substance that helps clean up free radicals.)
In 2010, however, MDA and the U.S. National Institutes of Health began conducting a large-scale study to probe the relationship between oxidative stress and ALS , with an eye to treatment development.
In 2013, the experimental drug dexpramipexole failed to show benefit  in a phase 3 trial conducted in 943 people with ALS in 11 countries. Dexpramipexole had demonstrated neuroprotective properties in laboratory experiments, and appeared to show dose-related slowing of functional decline in people with ALS in an earlier phase 2 trial. It was thought to work by improving mitochondrial function.
MDA-supported researchers continue to study mitochondrial dysfunction in ALS , with an eye to determining whether it's a cause or a consequence of motor neuron loss and whether restoring mitochondrial function can alter the ALS disease course.
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Stem cells can be thought of as cells that are in the very early stages of development, before they have become specialized (differentiated) to perform specific roles in tissues. They may be precursors to a specific cell types (such as muscle or nerve cells), or they may still retain pluripotency — the ability to develop into any of a number of different cell types.
In ALS, disease-affected stem cells  are being used as models in which to study disease processes and screen potential therapies. For example, in 2011, researchers created a model of a type of ALS  caused by mutations in the VAPB gene by causing skin cells from people with this form of the disease to revert to stem cells and then growing them in laboratory dishes.
Stem cells also are in development as cell-transplantation therapies. Theoretically, stem cells could be used to replace ALS-affected motor neurons; replace other types of cells, such as astrocytes; or release supportive proteins to help ailing nerve cells.
Early in 2012, the Israeli company BrainStorm Cell Therapeutics  announced that its NurOwn stem cell technology appears safe and appears to have improved breathing, swallowing and muscle strength  in four people with early-stage ALS, in a trial in Israel. In early 2013, BrainStorm, which plans to test its NurOwn stem cell technology  in a trial in the United States in people with ALS, has advanced its phase 1-2 safety trial of adult stem cells to a phase 2a dose-escalating trial .
Another biotechnology company, Neuralstem  reported in 2012 that its spinal cord stem cells, and the surgical technique used to transplant them, proved to be safe and well-tolerated  in a phase 1 clinical trial in 12 people with ALS. This first U.S.-based trial of neural stem cells in ALS opened at the MDA/ALS Center at Emory University in January 2010.
Many companies and institutions outside the United States (and a few inside) falsely advertise that they can cure ALS with stem cells . So far, there are no stem-cell-based treatments for ALS that are known to be either safe or effective, although Neuralstem's technology appears to be safe so far. Some companies may not even be injecting stem cells. Other may be using stem cells that are too undifferentiated and can be dangerous, while others may be using cells that are too differentiated and are no longer able to join existing tissues. Bottom line: Advertised stem cell therapies should be approached with great caution.
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Augie's Quest  is a concentrated MDA research initiative speeding the search for ALS treatments and a cure.
In 2007, MDA and Augie’s Quest joined forces with the ALS Therapy Development Institute (ALS TDI)  in Cambridge, Mass.
The multimillion-dollar partnership has created the largest ALS drug discovery project to date, which is conducting a thorough review of biochemical targets in ALS and drugs that may work on them.
Augie’s Quest funding enables ALS TDI to apply industrial-scale technology to ALS research in a way that has not been previously attempted.
In 2008, MDA established a nationwide consortium of five MDA-supported ALS centers  that would each receive $100,000 per year to fund the infrastructure necessary for collaboration on clinical trials in ALS. The centers are located in Atlanta, Boston, Houston, New York and San Francisco.
In early 2013, MDA launched a neuromuscular disease registry  through its national network of clinics. Through the registry, MDA aims to improve survival and quality of life for people with ALS and other neuromuscular diseases, and to expedite clinical trials and help make them more efficient. The Registry is being piloted at 25 MDA clinics to start; to learn more, check with your local MDA office.
In 2010, the U.S. Centers for Disease Control and Prevention opened the National ALS Registry  to compile a large database of information  about the incidence and prevalence of ALS, how the disease develops, and what types of treatments and interventions are beneficial.
People with ALS and/or their caregivers are encouraged to register at cdc.gov/als , where they will be asked to fill out short surveys about their and their families' health, their military background, and their environmental and occupational exposures.
In 2011, the ALS Research Collaboration, a University of Miami-based team dedicated to the study of familial (inherited) ALS, launched the fALS Connect  online familial ALS registry. The developers of this registry aim to connect families affected by familial ALS with scientists who study the disease , in an effort to accelerate development of treatments and cures. Membership is open to those who have familial ALS and their blood relatives.