Disease Modification in Severe Asthma: Reality or Utopia - European Medical Journal

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Disease Modification in Severe Asthma: Reality or Utopia

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In this interactive webinar, leading experts will examine whether disease modification in severe asthma is an achievable reality or remains a distant goal. The discussion will explore the evolving objectives of asthma management, from symptom relief to long-term disease control, and the potential for clinical remission through early intervention with biologics. Speakers will address key barriers to remission, including comorbidities, corticosteroid toxicity, and delayed treatment, and highlight the importance of individualised, multidimensional approaches. Finally, the session will consider the role of airway remodelling and Type 2 inflammation in disease progression, evaluating whether biologic therapies could alter the natural course of severe asthma. 

Speakers:

Alessandra Vultaggio1

Johann Christian Virchow2

Hitasha Rupani3,4

1. Careggi University Hospital in Florence, Italy
2. University of Rostock, Germany
3. University Hospital Southampton, UK
4. University of Southampton, UK 

Disclosures:

Vultaggio has been an advisor or speaker and received grants/research support from: ALK, Astra Zeneca, Bencard, GSK, Novartis, Sanofi-Genzyme, Stallergenes-Greer; and has been on advisory boards and received payments/honoraria for lectures from AstraZeneca, GSK, Sanofi, and Novartis.

Virchow has given independent lectures for and received honoraria from: ALK-Abello, Allergopharma, AstraZeneca, Avontec, Bayer, Bencard, Bionorica, Boehringer-Ingelheim, Chiesi, Essex/Schering-Plough, GSK, Janssen-Cilag, Leti, MEDA, Merck, MSD, Mundipharma, Novartis, Nycomed/Altana, Pfizer, Revotar, Sandoz-Hexal, Stallergens, TEVA, UCB/Schwarz-Pharma, Zydus/Cadila and possibly others; been on advisory boards and provided independent advice for ALK-Abello, Allergopharma, Avontec, Boehringer-Ingelheim, Chiesi, Essex/Schering-Plough, GSK, Janssen-Cilag, MEDA, MSD, Mundipharma, Novartis, Regeneron, Revotar, Roche, Sanofi-Aventis, Sandoz-Hexal, TEVA, UCB/Schwarz-Pharma and possibly others; received research grants from: Deutsche Forschungsgesellschaft, Land Mecklenburg-Vorpommern, GSK, MSD.

Rupani has received speaker and consultancy fees from AstraZeneca, GlaxoSmithKline, Teva, Novartis, and Chiesi; and has a research grant funded by GlaxoSmithKline. 

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or search for MHRA Yellowcard in the Google Play or Apple App Store. Adverse events should also be reported to GlaxoSmithKline on 0800 221 441e.

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