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The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development.
Orphanet J Rare Dis. 2015 Apr 23;10:49. doi: 10.1186/s13023-015-0258-1.
Orphanet J Rare Dis. 2015.
PMID: 25902795
Free PMC article.
Review.
A decade of optimizing drug development for rare neuromuscular disorders through TACT.
Wagner KR, De Luca A, Caizergues D, Dowling J, Goemans N, Gordish-Dressman H, Grounds MD, Kelly M, Mayhew A, McNally EM, Zoetis T, Lee J, Turner C, Wells DJ, Csimma C, Straub V.
Wagner KR, et al. Among authors: caizergues d.
Nat Rev Drug Discov. 2020 Jan;19(1):1-2. doi: 10.1038/d41573-019-00199-1.
Nat Rev Drug Discov. 2020.
PMID: 31907422
No abstract available.
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Report on the workshop: Meaningful outcome measures for Duchenne muscular dystrophy, London, UK, 30-31 January 2017.
Straub V, Mercuri E; DMD outcome measure study group.
Straub V, et al.
Neuromuscul Disord. 2018 Aug;28(8):690-701. doi: 10.1016/j.nmd.2018.05.013. Epub 2018 Jun 6.
Neuromuscul Disord. 2018.
PMID: 30033203
No abstract available.
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A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C.
Herson S, Hentati F, Rigolet A, Behin A, Romero NB, Leturcq F, Laforêt P, Maisonobe T, Amouri R, Haddad H, Audit M, Montus M, Masurier C, Gjata B, Georger C, Cheraï M, Carlier P, Hogrel JY, Herson A, Allenbach Y, Lemoine FM, Klatzmann D, Sweeney HL, Mulligan RC, Eymard B, Caizergues D, Voït T, Benveniste O.
Herson S, et al. Among authors: caizergues d.
Brain. 2012 Feb;135(Pt 2):483-92. doi: 10.1093/brain/awr342. Epub 2012 Jan 11.
Brain. 2012.
PMID: 22240777
Clinical Trial.
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