Clazakizumab

drug
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Also known as ALD-518ALD518BMS-945429

Summary

Clazakizumab (CHEMBL2108589) is a phase-3 clinical-stage antibody; indicated across 10 conditions including rheumatoid arthritis and crohn disease.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 10 conditions
  • Clinical trials: 18

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108589
NameClazakizumab
TypeAntibody
Max phase3

Also known as: ALD-518, ALD518, BMS-945429, Clazakizumab, CLAZAKIZUMAB

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

7 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
rheumatoid arthritis2MONDO:0008383EFO:0000685
Crohn disease2MONDO:0005011EFO:0000384
psoriatic arthritis2MONDO:0011849EFO:0003778
stomatitis2MONDO:0004842EFO:1001904
severe acute respiratory syndrome2MONDO:0005091MONDO:0100096
asthma2MONDO:0004979MONDO:0004979
graft versus host disease1MONDO:0013730EFO:0004599

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

Clinical trials

Total trials: 18.

Phase distribution

PhaseTrials
PHASE214
PHASE1/PHASE23
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03744910PHASE3TERMINATEDClazakizumab for the Treatment of Chronic Active Antibody Mediated Rejection in Kidney Transplant Recipients
NCT03380962PHASE1/PHASE2ACTIVE_NOT_RECRUITINGClazakizumab in Highly-HLA Sensitized Patients Awaiting Renal Transplant
NCT05727384PHASE2ACTIVE_NOT_RECRUITINGImproving Physical Function in Older Adults Using an Anti-inflammation Drug: The RIGHT Study
NCT00866970PHASE2COMPLETEDSafety, Efficacy and Pharmacokinetics of ALD518 in Patients With Non-Small Cell Lung Cancer-related Fatigue and Cachexia
NCT00867516PHASE2COMPLETEDSafety, Efficacy and Pharmacokinetics Study of ALD518 in Patients With Active Rheumatoid Arthritis
NCT01373151PHASE2COMPLETEDPhase IIB Rheumatoid Arthritis Dose Ranging Study for BMS-945429 in Subjects Who Are Not Responding to Methotrexate
NCT01403064PHASE2TERMINATEDSafety and Efficacy of ALD518 for Reducing Oral Mucositis in Head and Neck Cancer Subjects
NCT01490450PHASE2COMPLETEDPsoriatic Arthritis Dose Ranging Study for BMS-945429 in Subjects Who Are Not Responding to NSAIDs or Non-biologic Disease Modifying Anti-rheumatic Drugs (DMARDs) Therapy
NCT01530256PHASE1/PHASE2TERMINATEDExploratory Safety Study of ALD518 in Subjects With Steroid-refractory Acute Graft Versus Host Disease (GVHD)
NCT01545050PHASE2TERMINATEDDose Ranging Study of BMS-945429 in Subjects With Moderate to Severe Crohn’s Disease
NCT02015520PHASE2COMPLETEDPhase IIB Dose Ranging Study in Subjects With Moderate to Severe Rheumatoid Arthritis
NCT03380377PHASE1/PHASE2COMPLETEDClazakizumab for Chronic and Active Antibody Mediated Rejection Post-Kidney Transplant
NCT03444103PHASE2COMPLETEDA Pilot Trial of Clazakizumab in Late ABMR
NCT04129931PHASE2COMPLETEDPrecISE (Precision Interventions for Severe and/or Exacerbation-Prone Asthma) Network Study
NCT04343989PHASE2COMPLETEDA Randomized Placebo-controlled Safety and Dose-finding Study for the Use of the IL-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection
NCT04348500PHASE2COMPLETEDClazakizumab (Anti-Interleukin 6 (IL-6) Monoclonal) Compared to Placebo for Coronavirus Disease 2019 (COVID-19)
NCT04381052PHASE2TERMINATEDStudy for the Use of the IL-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection
NCT04494724PHASE2UNKNOWNClazakizumab vs. Placebo - COVID-19 Infection

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).