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Neurology· 2026Q1

Ofatumumab vs Ocrelizumab in Relapsing-Remitting Multiple Sclerosis

Sahla El Mahdaoui, Luigi Pontieri, Jeppe Romme Christensen, Hiba Alabdalridha et al.

Short summary

Ofatumumab showed a marginally increased annualized relapse rate (ARR) compared to ocrelizumab in relapsing-remitting MS (RRMS) patients (ARR rate ratio 1.18, p=0.018), though both therapies resulted in very low ARRs.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Ofatumumab showed a marginally increased annualized relapse rate (ARR) compared to ocrelizumab in RRMS patients (ARR rate ratio 1.18, p=0.018).
  • No significant differences were observed between ofatumumab and ocrelizumab for time to first relapse, disability worsening, progression independent of relapse activity, or MRI lesion activity.
  • Both therapies demonstrated very low ARR, indicating high effectiveness for both treatments.
  • The study was observational and acknowledges potential residual indication bias.

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND AND OBJECTIVES: B-cell-depleting therapy with anti-CD20 monoclonal antibodies is a highly effective and increasingly used treatment strategy for multiple sclerosis (MS); however, comparative effectiveness of anti-CD20 therapies is unclear. In this study, we aimed to evaluate the effectiveness of ofatumumab compared with ocrelizumab in relapsing-remitting MS (RRMS). METHODS: This was an observational cohort study based on data extracted from the Danish Multiple Sclerosis Registry. Patients with RRMS initiating ofatumumab or ocrelizumab treatment were included between January 2022 and November 2025. Primary outcomes were annualized relapse rate (ARR) rate ratio between the ofatumumab and ocrelizumab groups and hazard ratio (HR) for time to first relapse. Secondary outcomes were time to first 24-week confirmed disability worsening (CDW), progression independent of relapse activity (PIRA), and brain MRI lesion activity. We used the inverse probability of treatment weighting based on propensity scores to estimate the average treatment effects adjusted for baseline confounders. Main analyses followed an intention-to-treat (ITT) principle, with additional per-protocol (PP) analyses performed. RESULTS: = 0.018). The median follow-up time was 2.0 (interquartile range 1.3-2.7) years for the ofatumumab group and 2.5 (1.3-3.4) years for the ocrelizumab group. No statistically significant differences were found in the time to first relapse (HR 1.50, 95% CI 0.99-2.29), CDW (HR 0.83, 95% CI 0.58-1.20), PIRA (HR 0.78, 95% CI 0.53-1.15), or brain MRI lesion activity (HR 1.72, 95% CI 0.95-3.13). PP analyses yielded consistent results. DISCUSSION: The study indicates that ofatumumab treatment is associated with a marginally increased relapse rate compared with ocrelizumab treatment in patients with RRMS. However, the ARR was very low with both anti-CD20 therapies, and the difference is of limited clinical relevance. Important limitations include the observational design and the risk of residual indication bias. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that in patients with RRMS, ofatumumab is associated with a marginally increased ARR compared with ocrelizumab, with both drugs having very low ARRs.

The authors' abstract, as published at the source. Neurology, 2026 · DOI ↗

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Field: Pathology and Forensic Medicine

Pathology and Forensic MedicineMedicine