Satralizumab

drug
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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

FieldValue
ChEMBL IDCHEMBL3833307
NameSatralizumab
TypeAntibody
Max phase4
ATCL04AC19

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).

GeneTargetActionpAffinityCancer dependencyUniProt
Interleukin-6 receptorBinding8.85

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).

IndicationTrial phaseMONDOEFO
neuromyelitis optica4MONDO:0019100EFO:0004256
immune system disorder4MONDO:0005046EFO:0000540
myasthenia gravis3MONDO:0009688EFO:0004991
Japanese encephalitis3MONDO:0019209EFO:0007332
pulmonary arterial hypertension2MONDO:0015924EFO:0001361
Duchenne muscular dystrophy2MONDO:0010679MONDO: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

PhaseTrials
PHASE39
PHASE42
PHASE21
EARLY_PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07010302PHASE4NOT_YET_RECRUITINGRituximab Versus Ravulizumab, Inebilizumab, Satralizumab, and Eculizumab in NMOSD
NCT05269667PHASE4TERMINATEDA Study In Neuromyelitis Optica Spectrum Disorder (NMOSD) With Satralizumab As An Intervention
NCT05199688PHASE3RECRUITINGA Study To Evaluate Pharmacokinetics, Efficacy, Safety, Tolerability, And Pharmacodynamics Of Satralizumab In Pediatric Patients With Aquaporin-4 Antibody Positive Neuromyelitis Optica Spectrum Disorder (NMOSD)
NCT05271409PHASE3RECRUITINGA Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease
NCT05503264PHASE3RECRUITINGA 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
NCT05987423PHASE3ACTIVE_NOT_RECRUITINGStudy to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease
NCT06106828PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease
NCT02028884PHASE3COMPLETEDEfficacy and Safety Study of Satralizumab (SA237) as Add-on Therapy to Treat Participants With Neuromyelitis Optica (NMO) and NMO Spectrum Disorder (NMOSD)
NCT02073279PHASE3COMPLETEDEfficacy and Safety Study of Satralizumab (SA237) as Monotherapy to Treat Participants With Neuromyelitis Optica (NMO) and Neuromyelitis Optica Spectrum Disorder (NMOSD)
NCT04660539PHASE3COMPLETEDA Study to Evaluate the Safety and Efficacy of Satralizumab in Participants With Neuromyelitis Optica Spectrum Disorder (NMOSD)
NCT04963270PHASE3TERMINATEDA Study To Evaluate Efficacy, Safety, Pharmacokinetics, And Pharmacodynamics Of Satralizumab In Patients With Generalized Myasthenia Gravis
NCT06450639PHASE2ACTIVE_NOT_RECRUITINGA Study to Assess the Efficacy and Safety of Satralizumab in Duchenne Muscular Dystrophy (DMD)
NCT05727657EARLY_PHASE1WITHDRAWNSatralizumab in Aneurysmal Subarachnoid Hemorrhage
NCT06829524Not specifiedNOT_YET_RECRUITINGHANDLE-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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).