Therapeutic Potential of ATH434 in Multiple System Atrophy
Episode 126, Oct 18, 10:00 AM
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In this episode, Daniel Claaseen, MD, MS, a professor of neurology and chief of the Behavioral and Cognitive Neurology Division at Vanderbilt University Medical Center, offered his insight on phase 1/2 data that was recently presented at the International Parkinson and Movement Disorder Society (MDS) Congress on ATH434, an investigational drug in development from Alterity Therapeutics for multiple system atrophy (MSA). He dove into the therapy's mechanism of action and the currently known safety profile and considerations for its use, as well as the next steps in advancing care for patients with MSA as a whole.
Looking for more movement disorders discussion? Check out the NeurologyLive® movement disorder clinical focus page.
Episode Breakdown:
In this episode, Daniel Claaseen, MD, MS, a professor of neurology and chief of the Behavioral and Cognitive Neurology Division at Vanderbilt University Medical Center, offered his insight on phase 1/2 data that was recently presented at the International Parkinson and Movement Disorder Society (MDS) Congress on ATH434, an investigational drug in development from Alterity Therapeutics for multiple system atrophy (MSA). He dove into the therapy's mechanism of action and the currently known safety profile and considerations for its use, as well as the next steps in advancing care for patients with MSA as a whole.
Looking for more movement disorders discussion? Check out the NeurologyLive® movement disorder clinical focus page.
Episode Breakdown:
- 1:10 – Overviewing the conduct of the phase 1/2 studies
- 3:00 – Notable findings from data presented at MDS
- 4:30 – Mechanism of action behind ATH434
- 8:20 – Neurology News Minute
- 10:20 – Next steps in ATH434's development
- 11:15 – Current unmet needs for patients with MSA
The stories featured in this week's Neurology News Minute, which will give you quick updates on the following developments in neurology, are further detailed here:
FDA Removes Partial Hold for Myotonic Dystrophy Agent AOC 1001
FDA Approves Avadel's Sodium Oxybate for Cataplexy or Excessive Daytime Sleepiness in Pedatric Narcolepsy
FDA Approves AbbVie’s 24-Hour Foscarbidopa/Foslevodopa Pump for Advanced Parkinson Disease Treatment
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