Amyotrophic Lateral Sclerosis Drug Developers Set Their Sights on a New Treatment Target
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Amyotrophic Lateral Sclerosis Drug Developers Set Their Sights on a New Treatment Target

On March 22, 2023, via PRNewswire, the FDA announced that its CNS Drugs Advisory Committee voted unanimously in favor of a potential accelerated approval of tofersen to treat people with…

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Machine Learning Helps Identify Patterns of Progression in ALS
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Machine Learning Helps Identify Patterns of Progression in ALS

According to a story from myscience.org, neurodegenerative diseases, such as amyotrophic lateral sclerosis, are diseases that progressively worsen over time. However, progression in this disease is not consistent across all…

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A New Treatment for Amyotrophic Lateral Sclerosis Gets Approved, but Trial Results Are Spotty
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A New Treatment for Amyotrophic Lateral Sclerosis Gets Approved, but Trial Results Are Spotty

According to a story from CNN, a new treatment was recently approved by the US Food and Drug Administration (FDA) for amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's…

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Two Studies Lead to Possible Therapeutic Approach for Neurodegenerative Diseases
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Two Studies Lead to Possible Therapeutic Approach for Neurodegenerative Diseases

  The loss of axons (nervous system wiring) has been responsible for various neurodegenerative diseases such as peripheral neuropathies, Parkinson’s disease, glaucoma, and amyotrophic lateral sclerosis (ALS). According to a…

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Amyotrophic Lateral Sclerosis Patients Have an Alternative to Radicava ORS via IV
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Amyotrophic Lateral Sclerosis Patients Have an Alternative to Radicava ORS via IV

The new FDA-approved oral formulation of  Radicava ORS (edaravone) is more convenient than the intravenous formulation, yet the efficacy and composition remain the same. The oral formulation may also be…

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May is Amyotrophic Lateral Sclerosis Awareness Month: Spreading Rare Disease Awareness
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May is Amyotrophic Lateral Sclerosis Awareness Month: Spreading Rare Disease Awareness

According to a story from ALS News Today, around 5,000 people get diagnosed with amyotrophic lateral sclerosis (ALS) annually. In addition, costs of treatment for patients average $250,000 out of…

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Two ALS Studies May Unravel its Genetic Roots and Solve One of its Mysteries
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Two ALS Studies May Unravel its Genetic Roots and Solve One of its Mysteries

Scientists at London’s University College and a team of scientists at Stanford University simultaneously made the same discovery about amyotrophic lateral sclerosis (ALS): the genetic variant in the protein UNC13A…

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The House Passes a New Act Which Will Accelerate Research for ALS and Related Diseases
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The House Passes a New Act Which Will Accelerate Research for ALS and Related Diseases

Three organizations focused on amytrophic lateral sclerosis (ALS) as well as other rare neurodegenerative diseases, have just celebrated the House of Representatives' passage of the ACT for ALS (H.R.3537/S.1813). The…

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