Nemolizumab

drug
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Also known as CD14152CIM-331CIM331NemluvioNemolizumab-ilto

Summary

Nemolizumab (CHEMBL4297794) is an approved antibody (ATC D11AH12) targeting IL31RA; indicated across 5 conditions including prurigo and atopic eczema.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: D11AH12
  • Targets: 1 (IL31RA)
  • Indications: 5 conditions
  • Clinical trials: 23

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297794
NameNemolizumab
TypeAntibody
Max phase4
ATCD11AH12

Also known as: CD14152, CIM-331, CIM331, Nemluvio, Nemolizumab, Nemolizumab-ilto, NEMOLIZUMAB

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
IL31RAInterleukin-31 receptor, α subunitBinding8.70.7%Q8NI17

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): IL31RA.

Top Reactome pathways

1 total, by targets touching each:

PathwayTargetsGenes
IL-6-type cytokine receptor ligand interactions1IL31RA

Dominant GO biological processes

GO termTargets
MAPK cascade1
glandular epithelial cell differentiation1
acute inflammatory response to antigenic stimulus1
defense response1
cell surface receptor protein tyrosine kinase signaling pathway1
cell surface receptor signaling pathway via JAK-STAT1
positive regulation of cell population proliferation1
cytokine-mediated signaling pathway1
monocyte differentiation1
macrophage differentiation1
positive regulation of tyrosine phosphorylation of STAT protein1
homeostatic process1
negative regulation of macrophage activation1
negative regulation of apoptotic process1
positive regulation of DNA-templated transcription1

Indications & clinical

Indications

5 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
prurigo4MONDO:0021739MONDO:0021739
atopic eczema3MONDO:0004980EFO:0000274
systemic sclerosis2MONDO:0005100EFO:0000717
chronic kidney disease1MONDO:0005300EFO:0003884

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

Clinical trials

Total trials: 23.

Phase distribution

PhaseTrials
PHASE210
PHASE38
PHASE42
PHASE2/PHASE31
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07352566PHASE4NOT_YET_RECRUITINGUtilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT07396168PHASE4RECRUITINGNemolizumab to Treat Lichen Planopilaris, a Noncontrolled, Prospective, Pilot Study.
NCT03989206PHASE3ACTIVE_NOT_RECRUITINGLong-term Safety and Efficacy of Nemolizumab With Moderate-to-severe Atopic Dermatitis
NCT04204616PHASE3ACTIVE_NOT_RECRUITINGA Long-term Study of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)
NCT03985943PHASE3COMPLETEDEfficacy and Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis
NCT03989349PHASE3COMPLETEDEfficacy & Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis
NCT04501666PHASE3COMPLETEDStudy to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)
NCT04501679PHASE3COMPLETEDA Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)
NCT05052983PHASE3COMPLETEDA Study to Evaluate the Durability of Response and Safety of Nemolizumab for 24 Weeks in Participants With Prurigo Nodularis
NCT05056779PHASE3WITHDRAWNEfficacy and Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis With Inadequate Response to or for Whom Cyclosporine A is Not Medically Advisable
NCT05075408PHASE2/PHASE3COMPLETEDTo Evaluate the Efficacy and Safety of Nemolizumab for 12 Weeks in Participants With Chronic Kidney Disease With Associated Moderate to Severe Pruritus
NCT07047690PHASE2RECRUITINGA Study of Nemolizumab for the Treatment of Adults With Systemic Sclerosis
NCT07074977PHASE2RECRUITINGProof of Concept Study to Assess the Pharmacokinetics/Pharmacodynamics of Nemolizumab in Adults With Chronic Pruritus of Unknown Origin (CPUO)
NCT01986933PHASE2COMPLETEDA Phase 2 Study of CIM331 for Atopic Dermatitis Patients
NCT03100344PHASE2COMPLETEDDose-ranging Study of Nemolizumab in Atopic Dermatitis
NCT03181503PHASE2COMPLETEDSafety and Efficacy of Nemolizumab in PN
NCT03921411PHASE2COMPLETEDA Pharmacokinetics and Safety Study of Nemolizumab in Adolescent Participants With Atopic Dermatitis (AD)
NCT04365387PHASE2COMPLETEDA Study to Assess Immunization Responses in Adult and Adolescent Participants With Moderate-to-Severe Atopic Dermatitis Treated With Nemolizumab
NCT04562116PHASE2COMPLETEDA Study to Assess the Effects of Nemolizumab on Cytochrome P450 Substrates in Participants With Moderate-to-Severe Atopic Dermatitis
NCT04921345PHASE2COMPLETEDPharmacokinetics, Safety and Efficacy of Nemolizumab in Participants With Moderate-to-Severe Atopic Dermatitis
NCT05214794PHASE2COMPLETEDAn Open-label, Phase 2 Study to Assess the Efficacy and Safety of Nemolizumab in Subjects With Systemic Sclerosis
NCT05405985PHASE1COMPLETEDStudy to Access the Relative Bioavailability of Subcutaneous Dose of Nemolizumab When Administered Via Auto-Injector Versus Dual-Chamber Syringe
NCT03358693Not specifiedRECRUITINGMolecular Signatures in Inflammatory Skin Disease

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).