Satralizumab
drugOn this page
Also known as EnspryngRG6168SA-237SA237SapelizumabSatralizumab mwgeSatralizumab-mwge
Summary
Satralizumab (CHEMBL3833307) is an approved antibody (ATC L04AC19); indicated across 7 conditions including neuromyelitis optica and immune system disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Antibody
- ATC class: L04AC19
- Indications: 7 conditions
- Clinical trials: 14
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3833307 |
| Name | Satralizumab |
| Type | Antibody |
| Max phase | 4 |
| ATC | L04AC19 |
Also known as: Enspryng, RG6168, SA-237, SA237, Sapelizumab, Satralizumab, Satralizumab mwge, Satralizumab-mwge, SATRALIZUMAB
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| Interleukin-6 receptor | Binding | 8.85 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
7 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| neuromyelitis optica | 4 | MONDO:0019100 | EFO:0004256 |
| immune system disorder | 4 | MONDO:0005046 | EFO:0000540 |
| myasthenia gravis | 3 | MONDO:0009688 | EFO:0004991 |
| Japanese encephalitis | 3 | MONDO:0019209 | EFO:0007332 |
| pulmonary arterial hypertension | 2 | MONDO:0015924 | EFO:0001361 |
| Duchenne muscular dystrophy | 2 | MONDO:0010679 | MONDO:0010679 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 14.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 9 |
| PHASE4 | 2 |
| PHASE2 | 1 |
| EARLY_PHASE1 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT07010302 | PHASE4 | NOT_YET_RECRUITING | Rituximab Versus Ravulizumab, Inebilizumab, Satralizumab, and Eculizumab in NMOSD |
| NCT05269667 | PHASE4 | TERMINATED | A Study In Neuromyelitis Optica Spectrum Disorder (NMOSD) With Satralizumab As An Intervention |
| NCT05199688 | PHASE3 | RECRUITING | A Study To Evaluate Pharmacokinetics, Efficacy, Safety, Tolerability, And Pharmacodynamics Of Satralizumab In Pediatric Patients With Aquaporin-4 Antibody Positive Neuromyelitis Optica Spectrum Disorder (NMOSD) |
| NCT05271409 | PHASE3 | RECRUITING | A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease |
| NCT05503264 | PHASE3 | RECRUITING | A Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Satralizumab in Participants With Anti-N-methyl-D-aspartic Acid Receptor (NMDAR) or Anti-leucine-rich Glioma-inactivated 1 (LGI1) Encephalitis |
| NCT05987423 | PHASE3 | ACTIVE_NOT_RECRUITING | Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease |
| NCT06106828 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease |
| NCT02028884 | PHASE3 | COMPLETED | Efficacy and Safety Study of Satralizumab (SA237) as Add-on Therapy to Treat Participants With Neuromyelitis Optica (NMO) and NMO Spectrum Disorder (NMOSD) |
| NCT02073279 | PHASE3 | COMPLETED | Efficacy and Safety Study of Satralizumab (SA237) as Monotherapy to Treat Participants With Neuromyelitis Optica (NMO) and Neuromyelitis Optica Spectrum Disorder (NMOSD) |
| NCT04660539 | PHASE3 | COMPLETED | A Study to Evaluate the Safety and Efficacy of Satralizumab in Participants With Neuromyelitis Optica Spectrum Disorder (NMOSD) |
| NCT04963270 | PHASE3 | TERMINATED | A Study To Evaluate Efficacy, Safety, Pharmacokinetics, And Pharmacodynamics Of Satralizumab In Patients With Generalized Myasthenia Gravis |
| NCT06450639 | PHASE2 | ACTIVE_NOT_RECRUITING | A Study to Assess the Efficacy and Safety of Satralizumab in Duchenne Muscular Dystrophy (DMD) |
| NCT05727657 | EARLY_PHASE1 | WITHDRAWN | Satralizumab in Aneurysmal Subarachnoid Hemorrhage |
| NCT06829524 | Not specified | NOT_YET_RECRUITING | HANDLE-a Real World Study on Satralizumab in NMOSD |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).