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.
Study Design:
- Identify and extract the specific type of study design.
Patient Population Characteristics:
- Total number of patients
- Mean/median age
- Gender distribution
- Multiple sclerosis type
- Mean disease duration
- Baseline Expanded Disability Status Scale (EDSS) score
- Treatment-naive status vs. previous treatment history
Interventions Compared:
- Drug names
- Dosage (if specified)
- Treatment duration
- Number of patients in each treatment group
Annualized Relapse Rate (ARR):
- Baseline ARR
- On-treatment ARR
- Confidence intervals
- Statistical significance of differences between groups
Disability Progression:
- Method of measuring disability progression
- Percentage of patients with disability progression
- Changes in EDSS score
- Statistical significance of differences between groups
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
- Several studies of ocrelizumab included large sample sizes and long follow-up.
- The evidence base for ofatumumab is limited, with only a few small, short-term studies.