Ocrelizumab no evidence of disease activity (NEDA) status at 96 weeks in patients with relapsing multiple sclerosis: analysis of the phase III double-blind, double …

A Traboulsee, D Arnold, A Bar-Or, G Comi… - Neurology, 2016 - AAN Enterprises
Objective: To evaluate the effect of ocrelizumab vs interferon beta-1a (IFNβ-1a) on achieving
no evidence of disease activity (NEDA) in patients with relapsing MS over 96 weeks in two …

Efficacy of Ocrelizumab in Patients with Relapsing Multiple Sclerosis: Pooled Analysis of Two Identical Phase III, Double-Blind, Double-Dummy, Interferon Beta-1a …

S Hauser, D Arnold, A Bar-Or, G Comi, HP Hartung… - Neurology, 2016 - AAN Enterprises
Objective To evaluate the efficacy of ocrelizumab compared with interferon beta-1a (IFNβ-
1a) through pooled analysis of efficacy in OPERA I and OPERA II. Background MS …

No evidence of disease activity (NEDA) analysis by epochs in patients with relapsing multiple sclerosis treated with ocrelizumab vs interferon beta-1a

E Havrdová, DL Arnold, A Bar-Or… - Multiple Sclerosis …, 2018 - journals.sagepub.com
Background No evidence of disease activity (NEDA; defined as no 12-week confirmed
disability progression, no protocol-defined relapses, no new/enlarging T2 lesions and no T1 …

No Evidence of Disease Activity on Ocrelizumab Treatment in Patients With Early Relapsing Multiple Sclerosis: Pooled Analysis of the Phase III OPERA Studies (P4 …

E Havrdova, S Hauser, W Honeycutt, L Kappos… - 2017 - AAN Enterprises
Objective: To assess the proportion of patients with early relapsing multiple sclerosis (RMS)
with no evidence of disease activity (NEDA) following treatment with ocrelizumab vs …

annualized relapse rate and confirmed disability progression in patients receiving continuous ocrelizumab or switching from interferon beta-1a to ocrelizumab therapy …

S Hauser, B Brochet, X Montalban, R Naismith… - 2018 - AAN Enterprises
Objective: To assess the efficacy of switching to or maintaining ocrelizumab (OCR) therapy
on clinical measures of disease activity and progression in the open-label extension (OLE) …

Efficacy and safety of ocrelizumab in patients with relapsing-remitting multiple sclerosis with a suboptimal response to previous disease-modifying therapies (1‑year …

P Vermersch, JP Eralinna, R Nicholas… - Journal of the …, 2019 - jns-journal.com
Background The aim of the prospective, multicentre, single-arm Phase IIIb CASTING study
(NCT02861014) is to assess the efficacy/safety of ocrelizumab in patients with relapsing …

Efficacy and safety of ocrelizumab in patients with relapsing‐remitting multiple sclerosis with suboptimal response to prior disease‐modifying therapies: A primary …

P Vermersch, C Oreja‐Guevara, A Siva… - European Journal of …, 2022 - Wiley Online Library
Background and purpose Using the treatment goal of “no evidence of disease
activity”(NEDA) incorporating magnetic resonance imaging (MRI) re‐baselining, we aimed …

Week 144 results of a phase II, randomized, multicenter trial assessing the safety and efficacy of ocrelizumab in patients with relapsing–remitting multiple sclerosis …

S Hauser, D Li, P Calabresi, P O'Connor, A Bar-Or… - 2013 - AAN Enterprises
BACKGROUND: A Phase II RRMS trial showed that ocrelizumab (OCR) reduced Gd+
lesions by> 89% and annualized relapse rate (ARR) by> 73% vs placebo at Week 24. Week …

Five years of ocrelizumab in relapsing multiple sclerosis: OPERA studies open-label extension

SL Hauser, L Kappos, DL Arnold, A Bar-Or, B Brochet… - Neurology, 2020 - AAN Enterprises
Objective To assess over 3 years of follow-up the effects of maintaining or switching to
ocrelizumab (OCR) therapy on clinical and MRI outcomes and safety measures in the open …

A multicentre, open label, single-arm, phase 3b study (CONSONANCE) to assess the effectiveness and safety of ocrelizumab in patients with primary and secondary …

G Comi, R Bermel, A Bar-Or, M McGinley, D Arnold… - 2022 - AAN Enterprises
Objective: To report year-1 interim analysis results of the single-arm, phase 3b
CONSONANCE study (NCT03523858) designed to evaluate effectiveness and safety of …