Siltuximab

drug
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Also known as CLLB8CNTO-328CNTO328Sylvant

Summary

Siltuximab (CHEMBL1743070) is an approved antibody (ATC L04AC11); indicated across 18 conditions including immune system disorder and castleman disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L04AC11
  • Indications: 18 conditions
  • Clinical trials: 32

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1743070
NameSiltuximab
TypeAntibody
Max phase4
ATCL04AC11

Also known as: CLLB8, CNTO-328, CNTO328, Siltuximab, Sylvant, SILTUXIMAB

Targets

Targets

No target linkage available.

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

18 indications (3 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
immune system disorder4MONDO:0005046EFO:0000540
Castleman disease4MONDO:0015564EFO:1001332
plasma cell myeloma3MONDO:0009693EFO:0001378
severe acute respiratory syndrome3MONDO:0005091MONDO:0100096
myelodysplastic syndrome2MONDO:0018881EFO:0000198
prostate carcinoma2MONDO:0005159EFO:0001663
prostate adenocarcinoma2MONDO:0005082EFO:0000673
kidney cancer2MONDO:0002367MONDO:0002367
neoplasm2MONDO:0005070EFO:0000616
renal cell carcinoma1MONDO:0005086EFO:0000681
monoclonal gammopathy1MONDO:0004960EFO:0000203
acute myeloid leukemia1MONDO:0018874EFO:0000222
non-Hodgkin lymphoma1MONDO:0018908EFO:0005952
leukemia0MONDO:0005059EFO:0000565
type 1 diabetes mellitus0MONDO:0005147MONDO:0005147

3 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 32.

Phase distribution

PhaseTrials
PHASE217
PHASE16
PHASE1/PHASE23
EARLY_PHASE13
PHASE32
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07570173PHASE2/PHASE3RECRUITINGA Clinical Trial of MK-1045 in People With B-cell Acute Lymphoblastic Leukemia (MK-1045-005)
NCT04330638PHASE3COMPLETEDTreatment of COVID-19 Patients With Anti-interleukin Drugs
NCT04616586PHASE3TERMINATEDSILtuximab in Viral ARds (SILVAR) Study
NCT03315026PHASE2ACTIVE_NOT_RECRUITINGSiltuximab to Decrease Symptom Burden After Autologous Stem Cell Transplantation for Patients With Multiple Myeloma and AL Amyloidosis
NCT04975555PHASE2ACTIVE_NOT_RECRUITINGStudy to Evaluate the Role of Siltuximab in Treatment of Cytokine Release Syndrome (CRS) and Immune Effector Cell Associated Neurotoxicity (ICANS) Related to CAR-T Cell Therapy
NCT05684692PHASE2RECRUITINGScreening Trial for Pain Relief in Schwannomatosis (STARFISH)
NCT06470971PHASE2RECRUITINGSiltuximab for the Prevention of Severe Immune-Related Adverse Events During Immune Checkpoint Inhibitor Rechallenge in Patients With Advanced Cancer, CIRES Trial
NCT06679829PHASE2RECRUITINGA Study of Melphalan With or Without Siltuximab in People With Multiple Myeloma Having an Autologous Stem Cell Transplant
NCT07106671PHASE2RECRUITINGA Phase II Study of Siltuximab for CRS/ICANs After CAR-T in Multiple Myeloma
NCT00385827PHASE2TERMINATEDA Safety and Efficacy Study of Siltuximab (CNTO 328) in Male Subjects With Metastatic Hormone-Refractory Prostate Cancer (HRPC)
NCT00401843PHASE2COMPLETEDA Study of the Safety and Efficacy of CNTO 328 and Bortezomib to Bortezomib Alone in Patients With Relapsed or Refractory Multiple Myeloma
NCT00402181PHASE2COMPLETEDAn Efficacy and Safety Study of Siltuximab in Participants With Relapsed or Refractory Multiple Myeloma
NCT00911859PHASE2COMPLETEDA Study to Compare CNTO 328 (Anti-IL-6 Monoclonal Antibody) and VELCADE-Melphalan-Prednisone (VMP) With VMP Alone in Previously Untreated Multiple Myeloma Patients
NCT01024036PHASE2COMPLETEDA Study to Evaluate the Efficacy and Safety of CNTO328 Plus Best Supportive Care in Multicentric Castleman’s Disease
NCT01400503PHASE2COMPLETEDA Study to Evaluate the Safety of Long-term Treatment With Siltuximab in Patients With Multicentric Castleman’s Disease
NCT01484275PHASE2COMPLETEDA Study of Siltuximab (Anti- IL 6 Monoclonal Antibody) in Patients With High-risk Smoldering Multiple Myeloma
NCT01513317PHASE2TERMINATEDA Study Comparing Siltuximab Plus Best Supportive Care to Placebo Plus Best Supportive Care in Anemic Patients With International Prognostic Scoring System Low- or Intermediate-1-Risk Myelodysplastic Syndrome
NCT01531998PHASE1/PHASE2COMPLETEDLenalidomide/Bortezomib/Dexamethasone & CNTO 328 in Transplant Eligible Newly Diagnosed Multiple Myeloma (MM)
NCT02796859PHASE1/PHASE2UNKNOWNSiltuximab in Schizophrenia
NCT04191421PHASE1/PHASE2COMPLETEDSiltuximab and Spartalizumab in Patients With Metastatic Pancreatic Cancer
NCT04329650PHASE2COMPLETEDEfficacy and Safety of Siltuximab vs. Corticosteroids in Hospitalized Patients With COVID-19 Pneumonia
NCT04838860PHASE2TERMINATEDSiltuximab In Siltuximab-RElapsed/REfractory Multicentric CAstleman Disease
NCT06352866PHASE2WITHDRAWNSiltuximab for Cytokine Release Syndrome Prophylaxis Prior to tx w/ Teclistamab in RRMM
NCT06447376PHASE1RECRUITINGStudy of Cytokine Release Syndrome Prophylaxis and Treatment With Siltuximab Prior to Epcoritamab
NCT06990711PHASE1RECRUITINGA Phase 1 Clinical Trial of Siltuximab for the Treatment of Antibody-Mediated Rejection After Lung Transplantation
NCT01219010PHASE1COMPLETEDA Study Evaluating the Effects of Siltuximab on the Heart in Patients With Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
NCT01309412PHASE1TERMINATEDA Phase 1 Study of CNTO 328 (Siltuximab) in Relapsed or Refractory Multiple Myeloma
NCT05665725PHASE1COMPLETEDSiltuximab for the Prevention of CAR T Cell Related Cytokine Release Syndrome in Patients With CD19 Positive Non-Hodgkin Lymphoma
NCT05697510PHASE1UNKNOWNDose-escalation of Siltuximab in Combination With Idarubicin and Cytarabine Chemotherapy in Patients With Acute Myeloblastic Leukaemia (AML) With Poor Prognosis: SILTUXILAM
NCT02641522EARLY_PHASE1COMPLETEDModulation of STAT3 Signaling With Siltuximab in Type 1 Diabetes
NCT02805868EARLY_PHASE1WITHDRAWNSiltuximab in Treating Patients With Primary, Post-Polycythemia Vera, or Post-Essential Thrombocythemia Myelofibrosis
NCT05316116EARLY_PHASE1TERMINATEDSiltuximab in Large Granular Lymphocytic Leukemia (LGLL)

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).