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Time is Running out to Register at our Duchenne Muscular Dystrophy Industry Symposium

Home / TREAT-NMD Events and Masterclasses / Time is Running out to Register at our Duchenne Muscular Dystrophy Industry Symposium

Time is Running out to Register at our Duchenne Muscular Dystrophy Industry Symposium

Time is running out to register for our upcoming, expert-led, one-day symposium on Duchenne Muscular Dystrophy (DMD) on July 11, 2025, in Prague, Czechia. This event is aimed at industry professionals who are either new to working in Duchenne or lack a complete overview.

Symposium Focus

The symposium will delve into several pivotal areas:

  • Outcome Measures: Discussing the latest methodologies to assess DMD progression and treatment efficacy.
  • Genetic Advancements: Exploring breakthroughs in genetic research that could influence DMD therapies.
  • Treatment Advancements: Reviewing new therapeutic approaches and their clinical implications.
  • Internationally Recognised Standards of Care: Highlighting best practices in DMD patient management.

Objectives

The event aims to:

  • Equip participants with practical insights and tools applicable to their work in DMD.
  • Foster a collaborative environment for discussions, idea-sharing, and addressing challenges in the field.

Target Audience

This symposium is ideal for professionals in the pharmaceutical or biotech industries who are either new to the DMD field or seeking to broaden their knowledge. Attendees will have the opportunity to learn from key opinion leaders and gain a comprehensive overview of current DMD research and treatment landscapes.

You can view the programme for the event here: DMD Industry Day Draft Programme

Buy Tickets here
1 April 2025

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  • Home
  • Who We Are
    • About Us
    • Partnerships and Collaborations
    • Governance
    • Our Team
  • Who We Support
    • Patients
    • Clinicians / Researchers
    • Life Sciences Industry
  • What We Do
    • Advisory Committee for Therapeutics
      • Members of the Advisory Committee for Therapeutics
      • Take Part in TACT
      • Past Applicants
    • The Global Registry Network
      • Members of the Registry Network
    • Core Datasets
      • DM dataset
      • DMD dataset
      • FSHD dataset
      • LGMD
      • SMA
    • Education
      • Masterclasses and Events
      • Digital Resources
      • Endorsement of External Programmes
    • Post-Marketing Surveillance
  • Resources and Support
    • Neuromuscular Disease Information
      • Becker muscular dystrophy
      • Charcot-Marie-Tooth
      • Congenital muscular dystrophy
      • Congenital myasthenic syndromes
      • Duchenne muscular dystrophy
      • Facioscapulohumeral muscular dystrophy
      • GNE myopathy
      • Limb girdle muscular dystrophy
      • Myotonic dystrophy
      • Myotubular and centronuclear myopathies
      • Spinal muscular atrophy
    • Research Overview
      • DMD
        • Gene Therapy for DMD
        • Mutation Specific Approaches
        • Cell Therapy
        • Drug Therapy
    • Standards of Care & Family Guides
      • CM Care
      • CMD Care
      • DM Care
      • DMD Care
      • BMD Care
      • FSHD Care
      • SMA Care
    • SOP Library
      • MDX Mouse (DMD)
      • GRMD Dog (DMD)
      • CMD Mouse (CMD)
      • SMA Mouse (SMA)
      • CMD animal models
      • MDC1A Preclinical Research
      • Cell Lines
        • Clinical Outcome Measures
        • Functional Evaluation Tools
        • NMR (MRI/MRS) Imaging
        • Muscle Biopsy
    • Social and Ethical Issues
  • Conference
    • Registration
    • Sponsorship Opportunities
    • Conference Programme
    • Sponsors of the TREAT-NMD 8th International Conference
    • Programme Committee
    • Abstracts
    • Venue
  • News & Events
    • News
    • TREAT-NMD Events
    • All Events
    • Submit an Event
    • Newsletter Sign-up
    • Contact Us