NeurologyLive® Mind Moments‪®‬ NeurologyLive

Welcome to the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice.

In this episode, Ian Kremer, executive director of the leaders Engaged on Alzheimer's Disease (LEAD) coalition, spoke about several relevant topics regarding Alzheimer care as new novel therapeutics emerge. He talked about the lessons learned from the recent discontinuation of aducanumab, and the potential and limitations lecanemab (Leqembi; Eisai) and donanemab (Eli Lilly) may bring. Additionally, he provided comments about what matters to patients, the perception of the FDA approval process, and what is considered "clinically meaningful." Furthermore, he gave perspective on ways to improve drug development and emphasized the need for policy decisions to be based on scientific evidence and not by sensationalized headlines.

Looking for more Alzheimer disease/dementia discussion? Check out the NeurologyLive® Alzheimer disease/dementia clinical focus page.

Episode Breakdown:



1:10 – Promise in the Alzheimer field in 2024

4:05 – Ways of improving efficiencies with drug develpment

9:10 – Discontinuation of aducanumab

11:10– Neurology News Minute

13:50 – Lessons learned from aducanumab, antiamyloid therapies 

22:10– Conversations between clinicians and patients surrounding expectations/limitations of antiamyloid therapies and available treatments



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 Agrees to New Specialized Protocol for Phase 3b Study of ALS Agent NurOwn

FDA Approves Alternate Administration Routes for Antiseizure Medication Cenobamate

Extended Use of Investigational Agent IPX203 Safe in Parkinson Disease



Thanks for listening to the NeurologyLive® Mind Moments® podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.

Welcome to the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice.

In this episode, Francesco Saccà, MD, PhD, an associate professor of neurology at the University of Naples, discussed an ongoing study assessing the use of dimethyl fumarate, an approved therapy for relapsing multiple sclerosis, in patients with Friedreich ataxia (FA). He spoke on the mechanism of action of the agent and why it can be beneficial in this patient population, as well as how it differs from omaveloxolone (Skyclarys; Biogen), the first approved treatment for FA. In addition, he outlined the study design, the primary end point of frataxin decrease, and what would be considered a "successful" study. Furthermore, he spoke on the reasons behind the trial and what led investigators to this point.


Looking for more ataxia discussion? Check out the NeurologyLive® ataxia clinical focus page.

Episode Breakdown:



1:05 – Origin of the study

3:00 – Conduct of the study, end points, goals 

5:10 – Promising mechanism of action of dimethyl fumarate to treat Friedreich ataxia

7:30 – Questions in clinical impact of changes in frataxin

10:00 – Neurology News Minute

12:40 – What is considered a successful study?

14:55 – Patient inclusion, demographic makeup of the study

16:35 – Timeline of the trial and data readout



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 Approves Alexion's Ravulizumab-cwvz for Neuromyelitis Optica Spectrum Disorder
Epilepsy Agent STK-001 Demonstrates Disease-Modifying Effects in Early Phase Studies of Dravet Syndrome
Eisai Submits sBLA for Monthly Intravenous Maintenance Dosing of Alzheimer Therapy Lecanemab



Thanks for listening to the NeurologyLive® Mind Moments® podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.

Welcome to this special episode of the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice. For major FDA decisions in the field of neurology, we release short special episodes to offer a snapshot of the news, including the main takeaways for the clinical community, as well as highlights of the efficacy and safety profile of the agent in question.

In this episode, we're covering the recent approval of givinostat (Duvyzat; Italfarmaco) for the treatment of Duchenne muscular dystrophy (DMD). The therapy, a proprietary histone deacetylase (HDAC) inhibitor, was approved as the first nonsteroidal drug for patients with all genetic variants of DMD. The supporting data for the approval of givinostat comes from the phase 3 EPIDYS trial (NCT02851797). EPIDYS, a randomized, double-blind, placebo-controlled, multicenter study, included 179 ambulant male individuals who were randomly assigned 2:1 to either oral givinostat or placebo for an 18-month treatment period. Following the approval, Sharon Hesterlee, PhD, executive vice president and chief research officer of the Muscular Dystrophy Association, sat down to discuss the significance of the approval and how it changes the care for patients with DMD. She spoke specifically about the mechanism of action of the therapy, its safety profile, and how it may be used with other agents. In addition, she discussed other related topics on gene therapy and unmet needs for this patient population. 





For more of NeurologyLive's coverage of givinostat's approval, head here: FDA Approves Italfarmaco's Givinostat for Duchenne Muscular Dystrophy



Episode Breakdown:



0:30 – Givinostat approved for Duchenne muscular dystrophy

2:00 – Sharon Hesterlee, PhD, on the approval's implications

3:35 – Positive downstream effects of the approval

4:50 – Hersterlee on the safety profile of givinostat

5:40 – Promising outlook of the DMD field

6:45 – Overcoming roadblocks involved with gene therapy 

8:55 – Remaining unmet needs for patients with Duchenne

10:15 – Closing thoughts on the approval 



Thanks for listening to the NeurologyLive Mind Moments podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.

Welcome to the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice.

In this episode, Daniel Ontaneda, MD, an associate professor of neurology at the Cleveland Clinic Lerner College of Medicine, sat down to discuss the recently concluded Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) Forum. Ontaneda, program committee vice-chair of the meeting, provided insight on a number of notable sessions and discussions that highlighted the recent advances in the MS field. In addition, he talked about the need to innovate clinical trials, ways to tackle progressive MS, and whether drug trials are truly assessing patients at the right time points. Furthermore, he discussed multi-stage trials, the potential role of Bruton tyrosine kinase (BTK) inhibitors, and how this year's meeting differs from previous ones. 


Looking for more multiple sclerosis discussion? Check out the NeurologyLive® multiple sclerosis clinical focus page.

Episode Breakdown:



1:05 – Overviewing sessions from ACTRIMS Forum

13:10 – Innovating clinical trial design

16:15 – 2023 ACTRIMS vs 2024 ACTRIMS

20:20 – Neurology News Minute

23:30 – Testing combination approaches for progressive MS

26:45 – The impact of timing therapeutic interventions 



This episode is brought to you by Medical World News, a streaming channel from MJH Life Sciences®. Check out new content and shows every day, only at medicalworldnews.com.

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 AdComm to Review Investigational Alzheimer Agent Donanemab and Phase 3 Results

Amylyx Mulls Over Pulling AMX0035 Following Disappointing Phase 3 PHOENIX Findings

FDA Issues Complete Response Letter for Long-Acting Form of Glatiramer Acetate for Relapsing Multiple Sclerosis

Phase 2 PROCEED Trial of PACAP-Targeting Antibody Lu AG09222 in Migraine Announced



Thanks for listening to the NeurologyLive® Mind Moments® podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.

Welcome to the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice.

In this episode, Alcibiades Rodriguez, MD, medical director of the Comprehensive Epilepsy Center—Sleep Center at NYU Langone discussed several sleep-related topics, including the diagnosis of rare sleep disorders and hypersomnias. He spoke on the treatment of obstructive sleep apnea, the importance of adherence to medication, and the ways clinicians can help patients stick to their treatment regimen. Furthermore, he talked about the conversations between patients and clinicians to ensure an accurate diagnosis, as well as the emerging research in the sleep disorder field over the coming years.


Looking for more sleep disorders discussion? Check out the NeurologyLive® sleep disorders clinical focus page.

Episode Breakdown:



1:40 – Conversations needed to differentiate diagnoses

4:30 – Appearance of sleep disorders and overlap

6:50 – Complications with untreated sleep apnea

8:25 – Neurology News Minute

10:55 – Ways to improve adherence to medication

13:50 – Emerging research in the field



This episode is brought to you by Medical World News, a streaming channel from MJH Life Sciences®. Check out new content and shows every day, only at medicalworldnews.com.

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:





Glatiramer Acetate Depot Demonstrates Sustained Longterm Safety Profile as Potential MS Therapy

Phase 3 DAYBREAK Trial Highlights Long-Term Efficacy of Ozanimod for Relapsing Multiple Sclerosis

SRP-9001 Improves Duchenne Muscular Dystrophy Disease Trajectory Despite Failing to Meet Primary End Point in Phase 3 EMBARK Trial




Thanks for listening to the NeurologyLive® Mind Moments® podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.

Welcome to the NeurologyLive® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice.

In this episode, Stephen From, chief executive officer of Aruna Bio, sat down to discuss the company's investigational exosome candidate AB126 and its upcoming phase 1b/2a trial in patients with ischemic stroke. He discussed the mechanism of action of the therapy, the advantages of its anti-inflammatory and neuroprotective properties, and how it will be used with other stroke treatments. Furthermore, he gave insight on the complexities with conducting stroke trials and improving neurodegeneration in poststroke patients. 


Looking for more stroke discussion? Check out the NeurologyLive® stroke clinical focus page.

Episode Breakdown:



1:00 – Overviewing phase 1b/2a trial

7:05 – Mechanism of action of AB126

11:15 – Neurology News Minute

13:45 – Role of AB126 in stroke treatment landscape

17:50 – Challenges with repairing neurodegeneration in stroke



This episode is brought to you by Medical World News, a streaming channel from MJH Life Sciences®. Check out new content and shows every day, only at medicalworldnews.com.

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:





European Commission Approves Omaveloxolone as First Therapy for Friedreich Ataxia

AVP-786 Falls Short in Phase 3 Study of Alzheimer Disease Agitation

FDA Grants Priority Review to Efficacy Supplement for Sarepta Therapeutics’ SRP-9001 Indication Expansion




Thanks for listening to the NeurologyLive® Mind Moments® podcast. To support the show, be sure to rate, review, and subscribe wherever you listen to podcasts. For more neurology news and expert-driven content, visit neurologylive.com.