Satralizumab
Satralizumab (INN;[1] formerly sapelizumab; development code development code SA237) is a humanized monoclonal antibody that is being investigated for the treatment of neuromyelitis optica spectrum disorder.[2]
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | interleukin 6 receptor |
| Clinical data | |
| Other names | SA237 |
| ATC code |
|
| Identifiers | |
| CAS Number | |
| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C6340H9776N1684O2022S46 |
| Molar mass | 143416.47 g·mol−1 |
This drug is being developed by Chugai Pharmaceutical, a member of the Roche Group. As of 2018, satralizumab is undergoing Phase III trials.[3]
References
- World Health Organization (2015). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 114" (PDF). WHO Drug Information. 29 (4).
- Statement On A Nonproprietary Name Adopted By The USAN Council - Satralizumab, American Medical Association.
- "Chugai Presents Results from Phase III Study of Satralizumab in NMOSD at ECTRIMS 2018".
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