Elicit: Ocrelizumab vs Ofatumumab: Relapse and Disability Outcomes (public)

Ocrelizumab vs Ofatumumab: Relapse and Disability Outcomes (public)

What is the annualized relapse rate and confirmed disability progression with ocrelizumab vs ofatumumab in registry data?

In registry studies, ocrelizumab and ofatumumab show comparable annualized relapse rates (0.059 vs 0.038, p = 0.185) and both achieve 0% confirmed disability progression at 12 months.

Abstract

Registry studies in multiple sclerosis report that ocrelizumab and ofatumumab yield comparable outcomes. In one large, multicenter, propensity‐matched study (Zanghì et al., 2024), the annualized relapse rate was 0.059 with ocrelizumab versus 0.038 with ofatumumab (p = 0.185), and both treatments showed 0% confirmed disability progression over 12 months. A small post–natalizumab cohort (Cunha et al., 2025) likewise observed no significant change in relapse rate or in Expanded Disability Status Scale scores between ocrelizumab and ofatumumab. Other registry reports of ocrelizumab document relapse rates ranging from 0.014 to 0.11, with very low rates of confirmed disability progression over follow-up intervals from 6 months to several years.

These findings indicate that, based on available registry data, ocrelizumab and ofatumumab produce similar outcomes in annualized relapse rate and short-term disability progression among patients with multiple sclerosis.

Methods

We analyzed 40 sources from an initial pool of 999, using 8 screening criteria. Each paper was reviewed for 7 key aspects that mattered most to the research question.

Data extraction

We asked a large language model to extract each data column below from each paper.

Results

Characteristics of Included Studies

Study Study Design Registry Source Population Size Follow-up Duration
Zanghì et al., 2024 Retrospective cohort, multicenter, propensity-matched Italian multiple sclerosis centers 396 Mean 13.2 months
Zhu et al., 2022 Retrospective, multicenter, inverse probability of treatment weighting, registry MSBase 1045 ocrelizumab: median 1.8 years; cladribine: 1.1 years; natalizumab: 3.6 years
Cunha et al., 2025 Retrospective cohort Not mentioned 59 Not mentioned
Epstein et al., 2021 Retrospective chart review Not mentioned 56 2 years

Annualized Relapse Rate Results

Study Treatment Annualized Relapse Rate (95% CI) Study Population Effect Size
Zanghì et al., 2024 ocrelizumab: 0.059; ofatumumab: 0.038 (p=0.185) Relapsing multiple sclerosis No significant difference
Zhu et al., 2022 ocrelizumab: 0.07 (0.04–0.13) Relapsing-remitting multiple sclerosis post-fingolimod Ocrelizumab superior to cladribine, lower than natalizumab
Cunha et al., 2025 rituximab: 0.08 (post-switch); ocrelizumab/ofatumumab: no significant change Post-natalizumab No significant change for ocrelizumab/ofatumumab
Roos et al., 2024 ocrelizumab: 0.05; cladribine: 0.09 Relapsing-remitting multiple sclerosis Ocrelizumab superior to cladribine/fingolimod, similar to natalizumab/alemtuzumab

Confirmed Disability Progression Results

Study Treatment Confirmed Disability Progression Rate Time to Progression Statistical Significance
Zanghì et al., 2024 ocrelizumab/ofatumumab 0% 12 months No difference
Zhu et al., 2022 ocrelizumab/natalizumab No mention found No mention found No significant difference
Cunha et al., 2025 ocrelizumab/ofatumumab No significant change No mention found No significant difference for ocrelizumab/ofatumumab

Registry Data Considerations