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Targeting Huntingtin Expression in Patients with Huntington's Disease.

التفاصيل البيبلوغرافية
العنوان: Targeting Huntingtin Expression in Patients with Huntington's Disease.
المؤلفون: Tabrizi, Sarah J, Leavitt, Blair R, Rosser, Anne, Kordasiewicz, Holly B, Czech, Christian, Swayze, Eric E, Norris, Daniel A, Baumann, Tiffany, Gerlach, Irene, Schobel, Scott A, Paz, Erika, Smith, Anne V, Landwehrmeyer, G Bernhard, Bennett, C Frank, Lane, Roger M, Teams, Phase 1–2a IONIS-HTTRx Study Site, McColgan, Peter, Hensman, Davina, Ghosh, Rhia, Flower, Michael, Libri, Vincenzo, Saunders, Edwina, Raymond, Lynn, Wild, Edward J, Decolongon, Joji, Li, Tuan, Fathinia, Panteha, Lang, Christina, Lewerenz, Jan, Lindenberg, Katrin, Ludolph, Albert C, Schneider, Ariane, Trautmann, Sonja, Uhl, Stefanie, Saft, Carsten, Weydt, Patrick, Kaminski, Barbara, Kaminski, Daniela, Hoffmann, Rainer, von Hein, Sarah M, Muhlack, Siegfried, Gold, Ralf, Collins, Lucy, Mason, Sarah, Scott, Kirsten, Barker, Roger A, Stoker, Tom, Greenland, Julia, Andresen, Katie, Shanmugam, Mohan, Abdelghani, Mowafak, Turgut, Tolga, Peeren, Siofra, Colaco, Olga, Owens, Rebecca, Subin, Sujamole, Blair, Nick F, Spruth, Eike Jakob, Beckmann, Janna, Krug, Henriette, Langenfurth, Anika, Crossley, Diana, Akhtar, Nasreen, Gavin, Jennie, De Souza, Jenny, Massey, Thomas, McLauchlan, Duncan, Craufurd, David, Cousins, Rebecca, Shastin, Dmitri, Peall, Kathryn, Bhatt, Harsh, Davison, Andrew, Bagshawe, Joanne, Gunning, Belinda, Hamandi, Khalid, Priller, Josef, Rickards, Hugh
المصدر: The New England journal of medicine 380(24), 2307-2316 (2019). doi:10.1056/NEJMoa1900907
بيانات النشر: MMS
سنة النشر: 2019
مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adult, Dose-Response Relationship, Drug, Female, Humans, Huntingtin Protein: antagonists & inhibitors, Huntingtin Protein: cerebrospinal fluid, Huntingtin Protein: genetics, Huntington Disease: drug therapy, Injections, Spinal, Male, Middle Aged, Mutation, Nucleotides: chemical synthesis, Nucleotides: pharmacology, Oligonucleotides: cerebrospinal fluid, Oligonucleotides: therapeutic use, HTT protein, human, HTT(RX), Huntingtin Protein, Nucleotides, Oligonucleotides
جغرافية الموضوع: DE
الوصف: Huntington's disease is an autosomal-dominant neurodegenerative disease caused by CAG trinucleotide repeat expansion in HTT, resulting in a mutant huntingtin protein. IONIS-HTTRx (hereafter, HTTRx) is an antisense oligonucleotide designed to inhibit HTT messenger RNA and thereby reduce concentrations of mutant huntingtin.We conducted a randomized, double-blind, multiple-ascending-dose, phase 1-2a trial involving adults with early Huntington's disease. Patients were randomly assigned in a 3:1 ratio to receive HTTRx or placebo as a bolus intrathecal administration every 4 weeks for four doses. Dose selection was guided by a preclinical model in mice and nonhuman primates that related dose level to reduction in the concentration of huntingtin. The primary end point was safety. The secondary end point was HTTRx pharmacokinetics in cerebrospinal fluid (CSF). Prespecified exploratory end points included the concentration of mutant huntingtin in CSF.Of the 46 patients who were enrolled in the trial, 34 were randomly assigned to receive HTTRx (at ascending dose levels of 10 to 120 mg) and 12 were randomly assigned to receive placebo. Each patient received all four doses and completed the trial. Adverse events, all of grade 1 or 2, were reported in 98% of the patients. No serious adverse events were seen in HTTRx-treated patients. There were no clinically relevant adverse changes in laboratory variables. Predose (trough) concentrations of HTTRx in CSF showed dose dependence up to doses of 60 mg. HTTRx treatment resulted in a dose-dependent reduction in the concentration of mutant huntingtin in CSF (mean percentage change from baseline, 10% in the placebo group and -20%, -25%, -28%, -42%, and -38% in the HTTRx 10-mg, 30-mg, 60-mg, 90-mg, and 120-mg dose groups, respectively).Intrathecal administration of HTTRx to patients with early Huntington's disease was not accompanied by serious adverse events. We observed dose-dependent reductions in concentrations of mutant huntingtin. (Funded by Ionis Pharmaceuticals and F. ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:31059641; info:eu-repo/semantics/altIdentifier/issn/0028-4793; info:eu-repo/semantics/altIdentifier/issn/1533-4406; https://pub.dzne.de/record/140752Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-07074%22Test
الإتاحة: https://doi.org/10.1056/NEJMoa1900907Test
https://pub.dzne.de/record/140752Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-07074%22Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.69762C5E
قاعدة البيانات: BASE
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Mowafak ) ) ) [51] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Turgut, Tolga ) ) ) [52] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Peeren, Siofra ) ) ) [53] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Colaco, Olga ) ) ) [54] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Owens, Rebecca ) ) ) [55] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Subin, Sujamole ) ) ) [56] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Blair, Nick F ) ) ) [57] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Spruth, Eike Jakob ) ) ) [58] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Beckmann, Janna ) ) ) [59] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Krug, Henriette ) ) ) [60] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Langenfurth, Anika ) ) ) [61] => Array ( 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doi:10.1056/NEJMoa1900907 [Type] => main ) ) ) ) ) ) )
IllustrationInfo