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.

Perspectives on Best Practices for Gene Therapy Programs / Cheever, T.R., Berkley, D., Braun, S., Brown, R.H., Byrne, B.J., Chamberlain, J.S., Cwik, V., Duan, D., Federoff, H.J., High, K.A., Kaspar, B.K., Klinger, K.W., Larkindale, J., Lincecum, J., Mavilio, F., Mcdonald, C.L., Mclaughlin, J., Weiss Mcleod, B., Mendell, J.R., Nuckolls, G., et al.. - In: HUMAN GENE THERAPY. - ISSN 1043-0342. - 26:3(2015), pp. 127-133. [10.1089/hum.2014.147]

Perspectives on Best Practices for Gene Therapy Programs

MAVILIO, Fulvio;
2015

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.
Ahead Of Print from PubMed (19/10/2020)
2015
3-mar-2015
Inglese
26
3
127
133
7
http://online.liebertpub.com/doi/10.1089/hum.2014.147
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367233/pdf/hum.2014.147.pdf
Molecular Medicine; Molecular Biology; Genetics
reserved
info:eu-repo/semantics/article
Contributo su RIVISTA::Articolo su rivista
262
Perspectives on Best Practices for Gene Therapy Programs / Cheever, T.R., Berkley, D., Braun, S., Brown, R.H., Byrne, B.J., Chamberlain, J.S., Cwik, V., Duan, D., Federoff, H.J., High, K.A., Kaspar, B.K., Klinger, K.W., Larkindale, J., Lincecum, J., Mavilio, F., Mcdonald, C.L., Mclaughlin, J., Weiss Mcleod, B., Mendell, J.R., Nuckolls, G., et al.. - In: HUMAN GENE THERAPY. - ISSN 1043-0342. - 26:3(2015), pp. 127-133. [10.1089/hum.2014.147]
Cheever, Thomas R; Berkley, Dale; Braun, Serge; Brown, Robert H.; Byrne, Barry J.; Chamberlain, Jeffrey S.; Cwik, Valerie; Duan, Dongsheng; Federoff, ...espandi
28
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1074766
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