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BioWorld - Monday, July 20, 2026
Home » ALS

Articles Tagged with ''ALS''

Neurology/Psychiatric

Ractigen's therapeutic siRNA RAG-17 awarded US orphan drug designation for ALS

March 6, 2023
The FDA has awarded orphan drug designation...
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Neurology/Psychiatric

Blocking nuclear export of ALS/FTD troublemaker helps neurons survive

March 3, 2023
By Anette Breindl
Treatment with a cell-penetrating peptide that prevented nuclear export of unprocessed C9ORF72 RNA and its subsequent translation into neurotoxic dipeptide repeat proteins reduced motor neuron damage and death both in fruit fly models of amyotrophic lateral sclerosis (ALS), and in patient-derived induced neuronal precursor cells (iNPCs). The work suggests that targeting nuclear export could be a therapeutic option in ALS, and possibly also frontotemporal dementia (FTD), where C9ORF72 mutations also play a role.
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Brain and neural networks
Newco news

Newly public Coya takes on neurodegenerative disease with Tregs

Feb. 15, 2023
By Jennifer Boggs
Fresh off an end-of-year IPO, Coya Therapeutics Inc. is gearing up for clinical testing with its lead Treg-enhancing biologic in neurodegenerative disease, aiming to build on a wealth of academic-generated data highlighting the potential of Treg therapy to attack the neuroinflammation underlying diseases such as amyotrophic lateral sclerosis and Alzheimer’s disease.
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Illustration demonstrating muscle contraction in amyotrophic lateral sclerosis.
Neurology/Psychiatric

Cerevance expands series B financing to advance therapeutics for CNS diseases

Feb. 14, 2023
Cerevance Inc. has expanded its series B financing with an additional close of US$51 million, bringing the total series B financing to US$116 million. The proceeds will be used to advance Cerevance's therapeutics for central nervous system (CNS) diseases developed using its proprietary Nuclear Enriched Transcript Sort sequencing (Netsseq) platform.
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Conceptual 3D illustration showing degradation of motor neuron
Neurology/Psychiatric

SYF2 is novel target for neuronal survival in ALS

Feb. 6, 2023
By Mar de Miguel
The suppression of the SYF2 factor could be a new therapeutic strategy for the treatment of the different types of amyotrophic lateral sclerosis (ALS). According to a study from the University of Southern California, SYF2 acts on the TDP-43 protein, improving the survival of motor neurons affected by this disease. “We wanted to find something that would improve neuron survival across many different iPSC lines for ALS,” Justin Ichida told BioWorld.
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Brain and DNA
Biomarkers

NUP50 gene variation tied to ALS risk, researchers find

Jan. 26, 2023
Amyotrophic lateral sclerosis (ALS) is the most frequent adult-onset motor neuron disease, and it is pathologically related with frontotemporal dementia (FTD). Genetic studies have identified C9ORF72 as a major genetic cause of ALS/FTD. Further genetic analyses and validation studies have identified some other genes associated with ALS risk, highlighting among them the NUP50 gene, which encodes nuclear pore complex protein Nup50.
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Illustration demonstrating muscle contraction in amyotrophic lateral sclerosis.
Neurology/Psychiatric

Athira eyes IND filing this year for ATH-1105 for ALS

Jan. 9, 2023
Athira Pharma Inc. is advancing ATH-1105 toward a planned IND filing this year for first-in-human studies for amyotrophic lateral sclerosis (ALS).
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Neurology/Psychiatric

CRISPR/Cas9-based removal of a repeat expansion in C9ORF72 counteracts disease mechanisms

Dec. 15, 2022
The hexanucleotide repeat expansion (HRE) GGGGCC in the noncoding region of the chromosome 9 open reading frame 72 (C9ORF72) gene is the most common cause of hereditary (40%) and apparently sporadic (5%-6%) amyotrophic lateral sclerosis (ALS).
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Concept art for adeno-associated viral-based gene therapy.
Neurology/Psychiatric

Eikonoklastes and Forge Biologics partner on AAV manufacturing for ET-101 for ALS

Nov. 30, 2022
Eikonoklastes Therapeutics Inc. and Forge Biologics Inc. have established a manufacturing partnership to advance Eikonoklastes' adeno-associated viral (AAV)-based gene therapy, ET-101, into clinical trials for the treatment of patients with amyotrophic lateral sclerosis (ALS).
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Illustration demonstrating muscle contraction in amyotrophic lateral sclerosis.
Neurology/Psychiatric

Gene therapy ET-101 awarded orphan drug designation for ALS

Nov. 10, 2022
The FDA has awarded orphan drug designation to Eikonoklastes Therapeutics Inc.'s ET-101 program for the treatment of amyotrophic lateral sclerosis (ALS).
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