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AAN 2023

Coming soon
01:00 PM
Duration 12mins S5: Autoimmune Neurology: NMOSD and MG, A Focus On Treatment Trials
Long-term efficacy of satralizumab▼ in adults with AQP4-IgG-seropositive neuromyelitis optica spectrum disorder (NMOSD): Results from the roll-over, open-label study SAkuraMoon
A Traboulsee, I Kleiter, J Palace, K Fujihara, A Saiz, I Vodopivec, G Klingelschmitt, C Marcillat, J L. Bennett
02:48 PM
Duration 12mins S2:Child Neurology and Developmental Neurology
MANOEUVRE study design: A study of GYM329 (RO7204239) in patients with facioscapulohumeral muscular dystrophy (FSHD)
Statland J, Eichinger K, Morrow JM, Tasca G, Vissing J, Dodman A, Jaber B, Kletzl H, McIver T, Scalco RS, Yeung WY, Gaki E, Wagner KR
12:09 PM
Duration 7mins ES1: Emerging Science 1
Peripheral Blood Gene Expression Transcriptional Profiling Predicts Disease Progression in Primary Progressive Multiple Sclerosis
Gurevich M, Zilkcha-Falb R, Sonis P, Magalashvili D, Menascu S, Dolev M, Achiron A
01:24 PM
02:00 PM
Duration 12mins Boston Convention and Exhibition Center - 252AB
Enabling subcutaneous dosing of gantenerumab▼ in Alzheimer’s disease
Bittner B, Schwab D, Lott D, Boess F, Kohler R, Portron A, Wojtowicz J, Hofmann C
02:48 PM
Duration 12mins Boston, USA / Virtual (Hybrid)
Mattke S, Jun H, Chen E , Liu Y, Becker A, Wallick C
02:00 PM
Duration 12mins S26: Experimental Therapeutics in Dementia
ALUMNI AD STUDY DESIGN:Evaluation of Subcutaneous Gantenerumab in Historically Underrepresented US Populations With Early Symptomatic Alzheimer’s Disease
Seleri Assuncao S, Brangman S, Henderson J, Parker M, Monroe S, Mintzer J, Wise-Brown A, Grundman M, Smith J, Doody R, Lin H, Assman B, Rippon G
02:48 PM
Duration 12mins Boston Convention and Exhibition Center - 151AB
GRADUATE I and II: Findings of Two Phase III Randomized Placebo-controlled Studies Assessing the Efficacy and Safety of Subcutaneous Gantenerumab▼ in Early Alzheimer’s Disease (AD)
Smith J, Donohue MC, Gruendl E, Grimmer T, Perry RJ, Black SE, Salloway S, Lyons M, Rutten-Jacobs L, Bittner T, Blennow K, Pelentrides C, Barkhof F, Tonietto M, Baudler-Klein M, Fontoura P, Doody RS
04:30 PM
Duration 12mins S31: MS Clinical Decision Making and Special Populations
An Interim Analysis of Efficacy and Safety Data in Black and Hispanic Patients With Multiple Sclerosis Receiving Ocrelizumab▼ Treatment in the CHIMES Trial
Bernitsas E, Reder AT, Chinea A, Herrman C, O’Brien BC, Sater RA, Amezcua L, Williams MJ, Wu GF, Vartanian T, Pei J, Acosta J, Monson NL
02:36 PM
Duration 12mins S34:Child Neurology and Developmental Neurology
SUNFISH Parts 1 and 2: 4-year efficacy and safety of risdiplam▼ in Types 2 and 3 spinal muscular atrophy (SMA)
L Servais, M Oskoui, J W Day, N Deconinck, E S Mazzone, A Nascimento, K Saito, C Vuillerot, G Baranello, O Boespflug-Tanguy, N Goemans, J Kirschner, A Kostera-Pruszczyk, J Braid, G Papp, K Gorni, C Martin, R S Scalco, W Y Yeung, E Mercuri
01:12 PM
Duration 12mins S46: MS Therapeutics and Clinical Decision Making
Long-term Treatment with First-Line Ocrelizumab▼ in Patients with Early RMS: 9-Year Follow-Up Data From the OPERA Trial
Cerqueira J, Berthele A, Cree BAC, Filippi M, Pardo G, Pearson O, Traboulsee A, Ziemssen T, Vollmer T, Bernasconi C, Mandel C, Kulyk I, Chognot C, Schneble H-M, Prajapati K, Havrdova EK
01:24 PM
Duration 12mins S46: MS Therapeutics and Clinical Decision Making
Delayed Signs of Early Disability Progression After 8.5 Years of Ocrelizumab▼ Treatment in Patients With Relapsing Multiple Sclerosis
Weber MS, Kappos L, Hauser SL, Schneble HM, Wang Q, Giovannoni G
01:36 PM
Duration 12mins S46: MS Therapeutics and Clinical Decision Making
Low Disease Activity Over 4 Years of Ocrelizumab▼ Therapy in Treatment-Naive Patients With Early-Stage Relapsing-Remitting Multiple Sclerosis: The Phase IIIb ENSEMBLE Study
Bermel R, Hartung HP, Brochet B, Benedict R, Berger T, Carroll W, Vollmer T, Holmøy T, Karabudak R, Killestein J, Nos C, Patti F, Perrin Ross A, Vanopdenbosch L, Wuerfel J, Kuenzel T, Kadner K, Kulyk I, Freedman M
03:54 PM
Duration 12mins Session S48: Therapeutics for Muscle Disease
One-year Data from ENDEAVOR, a Phase 1b Trial of Delandistrogene Moxeparvovec (SRP-9001) in Patients with Duchenne Muscular Dystrophy (DMD)
Craig Zaidman, Crystal Proud, Craig McDonald, Stefanie Mason, Maitea Guridi, Shufang Wang, Carol Reid, Eddie Darton, Christoph Wandel, Sarah Lewis, Jyoti Malhotra, Danielle A. Griffin, Rachael A. Potter, Louise R. Rodino-Klapac, Jerry R. Mendell
04:06 PM
Duration 12mins Session S48: Therapeutics for Muscle Disease
A Phase 2 Clinical Trial Evaluating the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Patients with Duchenne Muscular Dystrophy (DMD)
Perry B. Shieh, Mendell JR, Sahenk Z, Lehman KJ, Lowes LP, Reash NF, Megan A. Iammarino, Lindsay N. Alfano, Brenna Sabo, Jeremy D. Woods, Christy L. Skura, Howard C. Mao, Loretta A. Staudt, Rachael A. Potter, Danielle A. Griffin, Sarah Lewis, Larry Hu, Teji Singh, Louise R. Rodino-Klapac
04:18 PM
04:30 PM
Duration 12mins Session S48: Therapeutics for Muscle Disease
Integrated Analyses of Data from Clinical Trials of Delandistrogene Moxeparvovec (SRP-9001) in Duchenne Muscular Dystrophy (DMD)
Craig Zaidman, Perry B. Shieh, Crystal Proud, Craig McDonald, John W. Day, Stefanie Mason, Maitea Guridi, Lixin Han, Lixi Yu, Carol Reid, Eddie Darton, Christoph Wandel, James Richardson, Jyoti Malhotra, Teji Singh, Louise R. Rodino-Klapac, Jerry R. Mendell