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Satralizumab

Alternative Names: satralizumab, sapelizumab, sa237, sa-237, enspryng, satralizumab-mwge, RG6168, RG 6168, RG-6168
Latest Update: 2025-03-18
Latest Update Note: Clinical Trial Update

Product Description

Satralizumab (Enspryng®), a humanized anti-interleukin-6 (IL-6) receptor monoclonal recycling antibody, has been developed by Chugai Pharmaceutical and Roche for the treatment of neuromyelitis optica spectrum disorder (NMOSD). (Sourced from: https://pubmed.ncbi.nlm.nih.gov/32797372/)

Mechanisms of Action: IL6 Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Approved

Approved Countries: Australia | Austria | Belgium | Brazil | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Ecuador | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | Indonesia | Ireland | Israel | Italy | Japan | Korea | Latvia | Lithuania | Malaysia | Netherlands | Norway | Peru | Poland | Portugal | Romania | Russia | Serbia | Singapore | Slovakia | Spain | Sweden | Switzerland | Taiwan | Turkey | Ukraine | United Arab Emirates | United States

Approved Indications: None

Known Adverse Events: None

Company: Hoffmann-La Roche
Company Location: BASEL SWITZERLAND V8
Company CEO: Severin Schwan
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Satralizumab

Countries in Clinic: Argentina, Australia, Austria, Brazil, Bulgaria, Canada, China, Croatia, Czech Republic, Denmark, France, Germany, Ghana, Hong Kong, Hungary, Israel, Italy, Japan, Korea, Malaysia, Netherlands, Poland, Portugal, Puerto Rico, Romania, Russia, Singapore, South Korea, Spain, Taiwan, Turkey, Ukraine, United Kingdom, United States

Active Clinical Trial Count: 26

Highest Development Phases

Phase 3: Encephalitis|Epilepsies, Partial|Graves Disease|Graves Ophthalmopathy|Myasthenia Gravis|Neuromyelitis Optica|Other|Thyroid Eye Disease|Thyroiditis, Autoimmune

Phase 2: Familial Primary Pulmonary Hypertension|Hypertension, Pulmonary|Muscular Dystrophy, Duchenne

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

WN41733

P3

Unknown Status

Neuromyelitis Optica

2029-02-28

jRCT2021220005

P3

Recruiting

Other

2028-04-30

WN43194

P3

Unknown Status

Other

2027-12-27

WN43174

P3

Unknown Status

Encephalitis

2027-12-07

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