@article{d7e487a171264ec6959d50fcde6dd468,
title = "Restoration of Nusinersen Levels Following Treatment Interruption in People With Spinal Muscular Atrophy: Simulations Based on a Population Pharmacokinetic Model",
abstract = "Background: Nusinersen is approved for the treatment of spinal muscular atrophy. The most common approved dosing regimen is four intrathecal loading doses of nusinersen 12 mg; the first three are administered at 14-day intervals followed by a fourth dose 30 days later, and then 12-mg maintenance doses are administered every 4 months thereafter. Interruption of nusinersen treatment in the maintenance dosing phase might occur for a number of clinical reasons. Objective: The objective of this report is to describe dosing regimens that allow for the most rapid restoration of steady-state concentrations of nusinersen in the cerebrospinal fluid (CSF) following a treatment interruption during maintenance dosing. Methods: Population pharmacokinetic models using integrated pharmacokinetic data from ten nusinersen clinical trials that included a broad range of participants with spinal muscular atrophy treated with intrathecal nusinersen were used to investigate different durations of treatment interruptions during maintenance treatment. Potential dosing regimens for re-initiation of nusinersen were evaluated, with the goal of achieving the quickest restoration of steady-state nusinersen CSF concentrations without exceeding maximal CSF exposures observed during the initial loading period. Results: Our pharmacokinetic modeling indicates the following regimen will lead to optimal restoration of nusinersen CSF levels after treatment interruption: two doses of nusinersen should be administered at 14-day intervals following treatment interruptions of ≥ 8 to < 16 months since the last dose, and three doses of nusinersen at 14-day intervals for treatment interruptions of ≥ 16 to < 40 months since the last maintenance dose, with subsequent maintenance dosing every 4 months in both instances. After treatment interruptions of ≥ 40 months, the full loading regimen will rapidly restore nusinersen CSF levels. Conclusions: Prolonged treatment interruptions lead to suboptimal CSF levels of nusinersen. The optimal regimen to restore nusinersen CSF levels depends on the interval since the last maintenance dose was administered.",
author = "Drew MacCannell and Zdenek Berger and Janbernd Kirschner and Eugenio Mercuri and Farrar, {Michelle A.} and Iannaccone, {Susan T.} and Kuntz, {Nancy L.} and Finkel, {Richard S.} and Marta Valente and Francesco Muntoni",
note = "Funding Information: Drew MacCannell, Zdenek Berger, and Marta Valente are full-time employees of and hold stock/stock options in Biogen. Janbernd Kirschner received funding for consultancy, educational, and research activities concerning SMA from AveXis/Novartis Gene Therapies, Biogen, Roche, and Scholar Rock. Eugenio Mercuri has participated in advisory boards for SMA studies for AveXis/Novartis Gene Therapies, Biogen, Ionis, Novartis, and Roche; is a principal investigator for ongoing Biogen/Ionis and Roche clinical trials; and has received funding from Famiglie SMA Italy, Italian Telethon, and SMA Europe. Michelle A. Farrar has participated in advisory boards for and received honoraria from Biogen, Roche, and Novartis. Susan T. Iannaccone receives partial salary support from the following grants: the Muscular Dystrophy Association, NeuroNEXT U24NS107176, NIH Wellstone Muscular Dystrophy Center P50HD087351, and Taysha Gene Therapies; receives research support from CureSMA, DoD W81XWH2010293, Parent Project for MD, and industry (Biogen, FibroGen, Novartis, PTC, ReveraGen, Sarepta, and Scholar Rock); and has served on medical advisory boards for Biogen, Novartis, and Sarepta. Nancy L. Kuntz has participated in advisory boards for argenx, Audentes, AveXis/Novartis Gene Therapies, Biogen, Cytokinetics, PTC, Roche, and Sarepta, and received honoraria from Biogen and clinical research funding direct to her institution from Audentes, AveXis/Novartis Gene Therapies, Biogen, and Sarepta. Richard S. Finkel has participated in SMA advisory boards for AveXis/Novartis Gene Therapies, Biogen, Roche, and Scholar Rock; received honoraria from AveXis/Novartis Gene Therapies, Biogen, Elsevier, Excerpta Medica, Roche, and Voyager; received research funding to institution from Biogen and Ionis for conduct of the CS3A, CHERISH, ENDEAR, NURTURE, and SHINE studies, and from AveXis/Novartis Gene Therapies, Cytokinetics, Roche, and Scholar Rock; was a member of the data safety monitoring boards for the AveXis AVX-101 phase I gene transfer study and the Roche Moonfish phase Ib study; serves in an advisory capacity for the nonprofit organizations Cure SMA, SMA Europe, SMA Foundation, and SMA Reach (UK); and receives royalty payments from the Children{\textquoteright}s Hospital of Philadelphia for licensing fees obtained for use of the CHOP INTEND motor function scale. Francesco Muntoni has participated in advisory boards for Biogen, Dyne Therapeutics, and Pfizer; has been a consultant for AveXis/Novartis Gene Therapies, Biogen, Roche, Santhera, and Sarepta; received grants from the European Commission, Muscular Dystrophy Association USA, Muscular Dystrophy UK, and Medical Research Council; received research funding/investigator grants from Biogen and Sarepta; and has been a principal investigator for Ionis nusinersen trials, the Roche olesoxime and risdiplam trials in SMA, and the Avexis/Novartis gene therapy trial of onasemnogene abeparvovec. Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
month = feb,
doi = "10.1007/s40263-022-00899-0",
language = "English (US)",
volume = "36",
pages = "181--190",
journal = "CNS Drugs",
issn = "1172-7047",
publisher = "Adis International Ltd",
number = "2",
}