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LIVE WEB STREAMING AVAILABLE ON SEPT. 27TH AND 28TH, 2010 LINKS
The meeting will consist of  four sessions:                                           
  •   Toxicology and Preclinical Findings to Date
  •   Biomarkers
  •   Clinical Trial Design / Endpoints
  •   Patient Registries and Assessing Long-Term Outcomes
Sept. 10 Registration is only for attendees not the Live Web.  

READ ON.............

Update on the Neuromuscular Stakeholders Meeting with FDA and NIH on AON Therapies


September 21, 2010 by CureDuchenne  


We are pleased to announce that the live web streaming links are now available for the FDA and NIH co-sponsored meeting    Antisense Oligonucleotide Therapies in Neuromuscular Diseases, taking place on the 27th and 28th September, 2010 in Washington DC, USA.

The collaborative meeting will engage over 100 stakeholders from multiple different neuromuscular diseases in which antisense oligonucleotides (AONs) are being explored as a therapeutic strategy (amyotrophic lateral sclerosis, Duchenne muscular dystrophy, myotonic dystrophy and spinal muscular atrophy). It is sponsored by Children's National Medical Centre, CureDuchenne, Foundation to Eradicate Duchenne, MDA, Parent Project Muscular Dystrophy and TREAT-NMD.

                                                                                                                                                                                                 The meeting will consist of  four sessions:                                           

  •   Toxicology and Preclinical Findings to Date
  •   Biomarkers
  •   Clinical Trial Design / Endpoints
  •   Patient Registries and Assessing Long-Term Outcomes

                                                                                                   Its goal is to allow stakeholders to explore potential pathways forward for the AONs with the eventual goal of creating a sound scientific foundation for neuromuscular disease clinical development programs. These initial discussions should be seen as first steps to help pave the way for future discussions and collaborations.

The agenda will be available in the near future at Cure Duchenne.org  website.

Over 100 stakeholders, consisting of researchers, academics, industry and patient group representatives, will participate in the meeting. In order to accommodate all those unable to attend the meeting due to space limitations or geographical distance, the whole meeting will be streamed on the web via dedicated web link(s).

To connect to the web streaming please use the links available here.

If you have any specific queries regarding this meeting please contact Emma Heslop (TREAT-NMD), Abby Bronson (CNMC) or John Porter (NIH).


For additional articles from Cure Duchenne Foundation, go to this link:http://www.cureduchenne.org/2010/09/update-on-the-neuromuscular-stakeholders-meeting-with-fda-and-nih-on-aon-therapies/
For a list of Duchenne Research and Trials go   Cure Duchenne Muscular Dystrophy Research Index