Our top coverage from this year’s Revolutionizing Atopic Dermatitis (RAD) conference highlighted the evolving therapy landscape for patients with AD.
Our top coverage featuring this year’s Revolutionizing Atopic Dermatitis (RAD) 2023 conference surrounded the unique and oftentimes challenging treatment landscape for patients with AD, as well as the disparities within dermatologic patient care that still need to be addressed.
These are your top RAD 2023 conference highlights. Click here for all our coverage from this conference.
Dr Larry Eichenfield: A Changing Therapy Landscape Provides More Options for Infants With AD
In this interview, Larry Eichenfield, MD, professor of dermatology and pediatrics and vice chair of the Department of Dermatology at the University of California San Diego School of Medicine, and chief of pediatric and adolescent dermatology at Rady Children's Hospital San Diego, shared key points he hoped physicians took away from his session on choosing the right treatments and therapies for AD in infants.
Posters Show Ruxolitinib Cream to Be Both Effective and Safe for Treating AD
Two posters provided insights into the safety and efficacy of ruxolitinib cream for AD and chronic hand dermatitis (CHD). The first poster analyzed safety reports during the first year of market approval, finding no systemic adverse events and a low incidence of application site reactions, indicating that ruxolitinib cream was well tolerated. The second poster presented interim results of a study testing the efficacy of ruxolitinib 1.5% cream in CHD, showing promising results with reductions in Investigator Global Assessment scores, hand eczema severity index, and itch levels after 4 weeks of treatment.
Symposium Highlights New Research on JAK, PDE-4 Inhibitors
In this symposium, Dr Eichenfield discussed innovations in nonsteroid topical therapies for AD, highlighting the efficacy and safety of topical ruxolitinib 1.5% cream in patients 12 years and older. Meanwhile, Jonathan Silverberg, MD, PhD, MPH, associate professor of dermatology and director of clinical research and contact dermatitis at The George Washington University School of Medicine and Health Sciences in Washington, DC, presented insights into oral Janus kinase (JAK) inhibitors for AD.
Panel Focuses on Burgeoning Therapies in Atopic Dermatitis
This symposium featured a panel discussing upcoming treatments for AD, including nonsteroidal topicals and biologics. Melinda Gooderham, MD, MSc, FRCPC, reviewed medications like tapinarof and roflumilast expected by 2024, presenting positive results from phase 3 trials, while David Rosmarin, MD, highlighted early-stage developments, emphasizing promising outcomes in treatments targeting microbial, itch, and adaptive immune system pathways for AD.
Disparities in AD Treatment: What Can Be Done?
The final symposium at RAD 2023 addressed disparities in care for patients of color with AD. Panelists, including Andrew Alexis, MD, MPH, FAAD, vice chair for diversity and inclusion for the Department of Dermatology and a dermatologist at the Center for Diverse Skin Complexions at Weill Cornell Medicine in New York City, highlighted the higher prevalence of diagnosed AD among patients of color and the impact on their quality of life.
STEER Data Open Door to SMA Gene Therapy for Wider Age Range of Children
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Navigating Sport-Related Neurospine Injuries, Surgery, and Managed Care
February 25th 2025On this episode of Managed Care Cast, we speak with Arthur L. Jenkins III, MD, FACS, CEO of Jenkins NeuroSpine, to explore the intersection of advanced surgical care for sport-related neurospine injuries and managed care systems.
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Neurologists Share Tips for Securing Patient Access to Gene Therapies
March 19th 2025Tenacious efforts at every level, from the individual clinician to the hospital to the state to Congress, will be needed to make sure patients can access life-saving gene therapies for neuromuscular diseases.
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EMBARK Data Show Continued Improvements With DMD Gene Therapy
March 19th 2025Data from the EMBARK trial of delandistrogene moxeparvovec in patients with Duchenne muscular dystrophy (DMD) show that benefits in functional outcomes, gene expression, and muscle imaging persist 2 years after receiving the gene therapy.
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How Access to SMA Treatment Varies Globally and by Insurance Type
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