Sixty-nine people living with ALS in Canada, Italy and Israel received either PrimeC or placebo for six months as part of the randomized portion of the trial, which is now complete. NeuroSense announced that it expects to release safety and clinical efficacy results next month.

Investigators at the University of Michigan have developed an environmental risk score based on a mixture of pesticides found in the blood. Greater exposure to these chemicals was associated with an increased risk of developing ALS.

More News:

BrainStorm Cell Therapeutics to Meet with FDA to Discuss Confirmatory Phase 3 Trial for NurOwn

Zydus Lifesciences Begins Phase 2 Clinical Trial of ZYIL1

NEAT1 Gene Variant May Advance ALS Onset by About 3 Years

Gene Activity Altered in Certain Brain Cells of People with C9-ALS

Botulinum Toxin Injection May Be a Treatment Option for Excess Saliva in People Living with ALS

Clinical trials and experimental treatments are often the first things that come to mind when thinking about ALS research. However, there are other types of research that contribute to our understanding of ALS and can be done from the comfort of your home.

ALS Focus is our patient- and caregiver-led survey program that asks people living with ALS and current and past caregivers about their needs and challenges so we can find solutions. By registering to participate in ALS Focus surveys and sharing your experiences, you can help strengthen care, accelerate therapy development, improve clinical trials, influence insurance coverage decisions and more.

Register to participate in future surveys HERE.

The ALS Association Welcomes 20th Class of Safenowitz Postdoctoral Fellows

Breaking Down Barriers for ALS: On the Quest for a Cure

Engaging the Whole World to End ALS

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Clinical research is the only way that promising laboratory science can be translated into treatments and cures for ALS and other neurological diseases. People with ALS, along with family members and caregivers, are essential partners in this research. For the most accurate and up-to-date information on both federally and privately funded clinical studies focusing on ALS and other similar motor neuron diseases, visit our website.

The National ALS Registry may be the single largest ALS research project ever created and is designed to identify ALS cases from throughout the entire United States. Every person living with ALS in the U.S. can take part, and there is no fee to participate. 

The ALS Association partners with the Northeast ALS Consortium (NEALS) to provide educational webinars for people with ALS, caregivers, and the broader ALS community. Topics include updates on clinical trials, best practices for clinical care, and current research efforts in ALS causes and treatments. 

For more details about current ALS research, our programs and awards, and the projects we fund, visit als.org/research.

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