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BioWorld - Tuesday, April 14, 2026
Home » ALS

Articles Tagged with ''ALS''

Health professional pointing stethoscope at Clinical Trial words, icons

Safety signal halts work on AB Science’s masitinib

June 1, 2021
By Richard Staines
Trading in shares in AB Science SA was suspended Tuesday after a safety signal prompted a voluntary hold on two late-stage clinical studies of its masitinib, in mastocytosis and amyotrophic lateral sclerosis, respectively.
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Walking with assistance

Orphazyme’s arimoclomol fails a phase III in ALS

May 7, 2021
By Lee Landenberger
Despite two recent clinical trial failures, Orphazyme A/S’s arimoclomol is still on track for its June 17 PDUFA date in treating Niemann-Pick disease type C. The newest stumble is in the pivotal study of arimoclomol for treating amyotrophic lateral sclerosis (ALS) as it failed to hit its primary and secondary endpoints.
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Brainstorm to brainstorm on BLA filing in ALS

Feb. 22, 2021
By Lee Landenberger
Brainstorm Cell Therapeutics Inc. said FDA senior leadership told the company the level of clinical data in the Nurown (neurotrophic factor-producing mesenchymal stem cells) phase III trial in amyotrophic lateral sclerosis (ALS) does not provide the threshold of substantial evidence needed to support a BLA.
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Brainstorm's Nurown falls short in phase III ALS trial

Nov. 17, 2020
By Michael Fitzhugh
Shares of Brainstorm Cell Therapeutics Inc. (NASDAQ:BCLI) fell 66.3% to $4.02 on Nov. 17 following news that its autologous cell therapy candidate, Nurown, missed the primary efficacy endpoint of a phase III amyotrophic lateral sclerosis (ALS) study.
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Brain and DNA

Study links two ALS mechanisms

Nov. 2, 2020
By John Fox
Mutations in the annexin A11 gene contribute to motor neuron degeneration in amyotrophic lateral sclerosis by disrupting cellular calcium ion homeostasis and stress granule protein disassembly contributing to ALS neurodegeneration.
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Macrophage illustration

Targeting periphery could be viable approach in ALS

Oct. 23, 2020
By Nuala Moran
French researchers have shown that modifying peripheral macrophages could quell microglial activation in the central nervous system, slowing the rate of decline and extending survival in mouse models of amyotrophic lateral sclerosis.
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Gene editing illustration

Starting with Biogen deal in ALS, Scribe planning a new chapter in CRISPR story

Oct. 6, 2020
By Cormac Sheridan
Scribe Therapeutics Inc., another CRISPR-based genome editing firm out of the Jennifer Doudna stable, launched with $20 million in series A funding and a deal with Biogen Inc. in amyotrophic lateral sclerosis (ALS), which brings in another $15 million up front and up to $400 million in development and commercial milestones.
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Isaac Veinbergs, CEO, Libra Therapeutics
Newco news

Libra launches with a $29M series A to treat neurodegenerative diseases

Sep. 23, 2020
By Lee Landenberger
In the past 10 years, the advances in understanding the etiology of neurodegenerative diseases have been dramatic. “The development of novel biomarkers and other tools as well are key in aiding diagnostic potential and the ability to track disease progression have been phenomenal,” Isaac Veinbergs, CEO of newly created Libra Therapeutics Inc., told BioWorld.
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Silhouette made of gears

Enclear scoops up $10M in series A funds for novel neurodegenerative disease treatment

Feb. 19, 2020
By Meg Bryant
Cambridge, Mass., startup Enclear Therapies Inc. has secured $10 million in series A financing led by 20/20 Healthcare Partners. The company is developing a device to aid in treating amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases by removing toxic proteins from cerebrospinal fluid (CSF).
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Brain

Breaching all three meninges improves drug delivery to brain

Dec. 27, 2019
By Anette Breindl
A single injection of SOD1-targeting RNA into the subpial space, which is below the innermost meningeal layer, was able to spread throughout the spinal cord and, via retrograde delivery, into brain centers that project to the spinal cord in several animal models, including primates.
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