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Report Overview

Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune condition that primarily affects the optic nerves and spinal cord. According to Edgar Carnero Contentti et al., 2025, the prevalence of NMOSD ranges from approximately 0.5-4 cases per 100,000 individuals worldwide. The disorder accounts for a significant burden in neuroimmunology, with growing focus on targeted immunotherapies. The NMOSD drug pipeline is expanding with advanced monoclonal antibodies and biologics aiming to reduce relapse rates and improve patient outcomes. According to the neuromyelitis optica spectrum disorder (NMOSD) pipeline analysis by Expert Market Research, the demand for NMOSD therapeutics are expected to grow steadily in the coming years.

  • Major companies involved in the neuromyelitis optica spectrum disorder (NMOSD) pipeline analysis include Beijing Mabworks Biotech Co., Ltd., along with Shanghai Jiaolian Drug Research and Development Co., among others.

  • Leading drugs currently in the pipeline include MIL62, BAT4406F, and others.

  • Robust NMOSD pipeline growth is driven by rising clinical trials for monoclonal antibodies, increasing R&D investments, and strategic collaborations to develop targeted immunotherapies and complement system inhibitors.

Report Coverage

The Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Analysis Report by Expert Market Research gives comprehensive insights into neuromyelitis optica spectrum disorder (NMOSD) therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for neuromyelitis optica spectrum disorder (NMOSD). The neuromyelitis optica spectrum disorder (NMOSD) report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The neuromyelitis optica spectrum disorder (NMOSD) pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with neuromyelitis optica spectrum disorder (NMOSD) treatment guidelines to ensure optimal care practices.

The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to neuromyelitis optica spectrum disorder (NMOSD).

Neuromyelitis Optica Spectrum Disorder Pipeline Analysis By Drug Class

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Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Outlook

Neuromyelitis optica spectrum disorder (NMOSD) is a rare, autoimmune condition that causes inflammation in the central nervous system, primarily affecting the optic nerves and spinal cord. It is often triggered by antibodies targeting aquaporin-4 (AQP4), leading to severe, recurrent relapses that may result in vision loss or paralysis.

Neuromyelitis optica spectrum disorder (NMOSD) treatments focus on relapse prevention and immune suppression. Therapies include corticosteroids, plasma exchange, and monoclonal antibodies such as eculizumab or inebilizumab, aiming to reduce disease activity and prevent long-term neurological damage. In March 2024, Ultomiris (ravulizumab-cwvz) was approved in the United States for anti-AQP4 antibody-positive NMOSD. The long-acting C5 complement inhibitor demonstrated a 98.6% relapse risk reduction in the CHAMPION-NMOSD Phase III trial.

Neuromyelitis Optica Spectrum Disorder (NMOSD) Epidemiology

According to Edgar Carnero Contentti et al., 2025, the global prevalence of neuromyelitis optica spectrum disorder (NMOSD) ranges from 0.5 to 4 per 100,000 individuals, with up to 10 per 100,000 in Asian and Afro-descendant populations. As per Farren B. S. Briggs et al., 2024, NMOSD prevalence in the United States is highest among black individuals (12.99/100,000). According to Caleb L. Shumway et al., 2024, NMOSD occurs predominantly in females (80%). These rising prevalence trends highlight a growing need for targeted therapies and robust drug pipeline expansion.

Neuromyelitis Optica Spectrum Disorder (NMOSD) – Pipeline Therapeutic Assessment

This section of the report covers the analysis of neuromyelitis optica spectrum disorder (NMOSD) drug candidates based on several segmentations, including:

By Phase

The pipeline assessment report covers 50+ drug analyses based on phase:

  • Late-Stage Products (Phase 3 and Phase 4)
  • Mid-Stage Products (Phase 2)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

By Drug Class

The neuromyelitis optica spectrum disorder (NMOSD) pipeline analysis report covers 50+ drug analyses based on drug classes:

  • Small Molecules
  • Monoclonal Antibodies
  • Gene Therapies
  • Peptides
  • Polymers

By Route of Administration

The pipeline assessment report covers 50+ drug analyses based on the route of administration.

  • Oral
  • Parenteral
  • Others

Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Assessment Segmentation, By Phases

The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total neuromyelitis optica spectrum disorder (NMOSD) clinical trials. It accounts for 35% of the pipeline, highlighting strong mid-stage development. Phase I and III each represent 22.5%, indicating balanced early and late-stage innovations. This robust pipeline fosters continued therapeutic advancement and future market expansion in NMOSD treatment.

Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Assessment Segmentation, By Drug Classes

The drug molecule categories covered under the neuromyelitis optica spectrum disorder (NMOSD) pipeline analysis include small molecules, monoclonal antibodies, gene therapies, peptides, and polymers. The neuromyelitis optica spectrum disorder (NMOSD) report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for neuromyelitis optica spectrum disorder (NMOSD). C5 complement inhibition therapies are rapidly advancing in the neuromyelitis optica spectrum disorder (NMOSD) drug pipeline. For instance, eculizumab, the first FDA-approved C5 inhibitor, has demonstrated significant relapse reduction in AQP-4 antibody-positive patients. Additionally, ravulizumab-cwvz, a long-acting C5 inhibitor, is under evaluation and has shown no relapses in phase 3 trials, offering a promising treatment option with extended dosing intervals for improved patient convenience.

Neuromyelitis Optica Spectrum Disorder (NMOSD) Clinical Trials – Key Players

The EMR report for the neuromyelitis optica spectrum disorder (NMOSD) pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed neuromyelitis optica spectrum disorder (NMOSD) therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in neuromyelitis optica spectrum disorder (NMOSD) clinical trials:

  • Beijing Mabworks Biotech Co., Ltd.
  • Shanghai Jiaolian Drug Research and Development Co., Ltd.
  • Bio-Thera Solutions
  • ImmuneCare Biopharmaceuticals (Shanghai) Co., Ltd.
  • Nanjing IASO Biotechnology Co., Ltd.
  • Amgen
  • Biocad
  • RemeGen Co., Ltd.
  • Hoffmann-La Roche
  • AstraZeneca
  • Alexion Pharmaceuticals, Inc.
  • AbelZeta Pharma Inc.

Neuromyelitis Optica Spectrum Disorder (NMOSD) – Emerging Drugs Profile

This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for neuromyelitis optica spectrum disorder (NMOSD). It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of neuromyelitis optica spectrum disorder (NMOSD) drug candidates.

Drug: MIL62

MIL62, sponsored by Beijing Mabworks Biotech Co., Ltd., is currently undergoing a Phase Ib/III clinical trial to evaluate its safety and efficacy in patients with neuromyelitis optica spectrum disorder (NMOSD). This study aims to assess how well MIL62, a third-generation anti-CD20 antibody, performs in reducing NMOSD relapses. Developed using an ADCC-enhanced antibody platform, MIL62 targets B cells and holds multiple patents globally. The drug is showing promise across autoimmune and oncology indications and is being positioned as a potential treatment alternative for serious, life-threatening disorders.

Drug: BAT4406F

BAT4406F is an ADCC-enhanced, fully humanized anti-CD20 monoclonal antibody currently being evaluated by Bio-Thera Solutions in a Phase II/III trial for patients with neuromyelitis optica spectrum disorder (NMOSD) who test positive for aquaporin-4 antibodies. The study is aiming to assess the drug’s efficacy and safety through a randomized, double-blind, placebo-controlled design. BAT4406F is being administered intravenously at 500 mg on Day 1 and Day 182.

*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*

Key Questions Answered in the Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Insight Report

  • Which companies/institutions are leading the neuromyelitis optica spectrum disorder (NMOSD) drug development?
  • What is the efficacy and safety profile of neuromyelitis optica spectrum disorder (NMOSD) pipeline drugs?
  • Which company is leading the neuromyelitis optica spectrum disorder (NMOSD) pipeline development activities?
  • What is the current neuromyelitis optica spectrum disorder (NMOSD) commercial assessment?
  • What are the opportunities and challenges present in the neuromyelitis optica spectrum disorder (NMOSD) pipeline landscape?
  • Which company is conducting major trials for neuromyelitis optica spectrum disorder (NMOSD) drugs?
  • Which companies/institutions are involved in neuromyelitis optica spectrum disorder (NMOSD) collaborations aimed at providing enhanced therapeutic alternatives for patients?
  • What are the geographies covered for clinical trials in neuromyelitis optica spectrum disorder (NMOSD)?

Reasons To Buy This Report

The Neuromyelitis Optica Spectrum Disorder (NMOSD) Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for neuromyelitis optica spectrum disorder (NMOSD). It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into neuromyelitis optica spectrum disorder (NMOSD) collaborations, regulatory environments, and potential growth opportunities.

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Key Highlights of the Report

Please note that the figures mentioned in the description serve as estimates and may vary from the actual figures presented in the final report.

Scope of the Report

Details

Drug Pipeline by Clinical Trial Phase

  • Late-Stage Products (Phase III and Phase IV)
  • Mid-Stage Products (Phase II)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

Route of Administration

  • Oral
  • Parenteral
  • Others

Drug Classes

  • Small Molecules
  • Monoclonal Antibodies
  • Gene Therapies
  • Peptides
  • Polymers

Leading Sponsors Covered

  • Beijing Mabworks Biotech Co., Ltd.
  • Shanghai Jiaolian Drug Research and Development Co., Ltd.
  • Bio-Thera Solutions
  • ImmuneCare Biopharmaceuticals (Shanghai) Co., Ltd.
  • Nanjing IASO Biotechnology Co., Ltd.
  • Amgen
  • Biocad
  • RemeGen Co., Ltd.
  • Hoffmann-La Roche
  • AstraZeneca
  • Alexion Pharmaceuticals, Inc.
  • AbelZeta Pharma Inc.

Geographies Covered

  • North America
  • Europe
  • Asia Pacific
  • Others

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