# Comparative Efficacy of Ublitixumab Versus Natalizumab in the Treatment of Relapsing and Remitting Multiple Sclerosis

**Authors:** Sai V Chitturi, Jonnalagadda Amith Priyansu, Akhil Sadhu, Hemanthi Ramisetty, Manoj R Pallapothu, Deepiikha Kogantii

PMC · DOI: 10.7759/cureus.95422 · 2025-10-26

## TL;DR

This review compares ublituximab and natalizumab for treating relapsing-remitting multiple sclerosis, focusing on their effectiveness and safety.

## Contribution

The paper provides a comparative analysis of two monoclonal antibodies for RRMS, highlighting their unique therapeutic roles.

## Key findings

- Ublitixumab and natalizumab have distinct mechanisms of action and safety profiles.
- Both drugs reduce relapse frequency and slow disability progression in RRMS patients.
- The review supports individualized treatment strategies based on patient-specific factors.

## Abstract

Relapsing-remitting multiple sclerosis (RRMS) is a chronic autoimmune disorder characterized by immune-mediated demyelination and neurodegeneration, leading to progressive neurological impairment. Disease-modifying therapies (DMTs) play a crucial role in managing RRMS by reducing relapse frequency and slowing disability progression. Among these, monoclonal antibodies such as ublituximab and natalizumab have emerged as key therapeutic options with distinct mechanisms of action and safety profiles. This narrative review aims to compare the efficacy, safety, and clinical impact of ublituximab and natalizumab in the treatment of RRMS, providing insights into their role in individualized treatment strategies.

## Linked entities

- **Diseases:** relapsing-remitting multiple sclerosis (MONDO:0005314), multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** neurodegeneration (MESH:D019636), RRMS (MESH:D020529), autoimmune disorder (MESH:D001327), neurological impairment (MESH:D009422), Multiple Sclerosis (MESH:D009103), demyelination (MESH:D003711)
- **Chemicals:** ublituximab (MESH:C000619007), Natalizumab (MESH:D000069442), Ublitixumab (-)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12648440/full.md

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Source: https://tomesphere.com/paper/PMC12648440