| Literature DB >> 25654329 |
Thomas R Cheever1, Dale Berkley, Serge Braun, Robert H Brown, Barry J Byrne, Jeffrey S Chamberlain, Valerie Cwik, Dongsheng Duan, Howard J Federoff, Katherine A High, Brian K Kaspar, Katherine W Klinger, Jane Larkindale, John Lincecum, Fulvio Mavilio, Cheryl L McDonald, James McLaughlin, Bonnie Weiss McLeod, Jerry R Mendell, Glen Nuckolls, Hansell H Stedman, Danilo A Tagle, Luk H Vandenberghe, Hao Wang, Pamela J Wernett, James M Wilson, John D Porter, Amelie K Gubitz.
Abstract
With recent successes in gene therapy trials for hemophilia and retinal diseases, the promise and prospects for gene therapy are once again garnering significant attention. To build on this momentum, the National Institute of Neurological Disorders and Stroke and the Muscular Dystrophy Association jointly hosted a workshop in April 2014 on "Best Practices for Gene Therapy Programs," with a focus on neuromuscular disorders. Workshop participants included researchers from academia and industry as well as representatives from the regulatory, legal, and patient advocacy sectors to cover the gamut from preclinical optimization to intellectual property concerns and regulatory approval. The workshop focused on three key issues in the field: (1) establishing adequate scientific premise for clinical trials in gene therapy, (2) addressing regulatory process issues, and (3) intellectual property and commercialization issues as they relate to gene therapy. The outcomes from the discussions at this workshop are intended to provide guidance for researchers and funders in the gene therapy field.Entities:
Mesh:
Year: 2015 PMID: 25654329 PMCID: PMC4367233 DOI: 10.1089/hum.2014.147
Source DB: PubMed Journal: Hum Gene Ther ISSN: 1043-0342 Impact factor: 5.695