Bimekizumab

drug
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Also known as Bimekizumab-bkzxBimzelxUCB-4940Ucb4940

Summary

Bimekizumab (CHEMBL4297700) is an approved antibody (ATC L04AC21); indicated across 7 conditions including psoriasis and immune system disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L04AC21
  • Indications: 7 conditions
  • Clinical trials: 52

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297700
NameBimekizumab
TypeAntibody
Max phase4
ATCL04AC21

Also known as: Bimekizumab, Bimekizumab-bkzx, Bimzelx, UCB-4940, Ucb4940, UCB4940, BIMEKIZUMAB

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 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
psoriasis4MONDO:0005083EFO:0000676
immune system disorder4MONDO:0005046EFO:0000540
parapsoriasis4MONDO:0006592EFO:1000747
psoriatic arthritis3MONDO:0011849EFO:0003778
ankylosing spondylitis3MONDO:0005306EFO:0003898
hidradenitis suppurativa3MONDO:0006559EFO:1000710
rheumatoid arthritis2MONDO:0008383EFO:0000685

Clinical trials

Total trials: 52.

Phase distribution

PhaseTrials
PHASE324
PHASE214
PHASE18
PHASE45
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07352566PHASE4NOT_YET_RECRUITINGUtilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT07497620PHASE4NOT_YET_RECRUITINGBimzelx (Bimekizumab) For The Treatment Of Adult Onset PRP
NCT04340076PHASE4COMPLETEDDose Reduction of IL17 and IL23 Inhibitors in Psoriasis
NCT05499416PHASE4WITHDRAWNEffect of Bimekizumab in Patients With Psoriasis Vulgaris and Active Psoriatic Arthritis
NCT06336343PHASE4COMPLETEDBimekizumab in Plaque Psoriasis
NCT04009499PHASE3ACTIVE_NOT_RECRUITINGA Study to Assess the Long-term Safety, Tolerability, and Efficacy of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis
NCT04436640PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Subjects With Active Axial Spondyloarthritis Including Ankylosing Spondylitis and Nonradiographic Axial Spondyloarthritis
NCT04901195PHASE3ACTIVE_NOT_RECRUITINGA Study to Test the Long-term Treatment of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa
NCT06425549PHASE3RECRUITINGA Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Ustekinumab in Children and Adolescents From 6 Years to Less Than 18 Years of Age With Moderate to Severe Plaque Psoriasis
NCT06506916PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Effect of Bimekizumab on Gene Expression Biomarkers in Study Participants With Moderate to Severe Plaque Psoriasis
NCT06624228PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Study Participants With Active Psoriatic Arthritis
NCT06668181PHASE3RECRUITINGAn Open-label Study to Evaluate the Pharmacokinetics and Safety of Bimekizumab in Pediatric Study Participants With Active Juvenile Idiopathic Arthritis Subtypes Enthesitis-related Arthritis (Including Juvenile-onset Ankylosing Spondylitis) and Juvenile Psoriatic Arthritis
NCT06921850PHASE3RECRUITINGA Study to Assess the Pharmacokinetics and Safety of Bimekizumab in Children and Adolescents With Moderate to Severe Hidradenitis Suppurativa
NCT07219420PHASE3RECRUITINGA Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Palmoplantar Pustulosis
NCT03370133PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Placebo and an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT03410992PHASE3COMPLETEDA Study With a Initial Treatment Period Followed by a Randomized-withdrawal Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT03412747PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT03536884PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT03598790PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT03766685PHASE3COMPLETEDA Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or the Auto-injector for the Subcutaneous Self-injection of Bimekizumab Solution by Subjects With Moderate to Severe Chronic Plaque Psoriasis (PSO)
NCT03895203PHASE3COMPLETEDA Study to Test the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis
NCT03896581PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis
NCT03928704PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Nonradiographic Axial Spondyloarthritis
NCT03928743PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Ankylosing Spondylitis
NCT04109976PHASE3COMPLETEDA Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or the Auto-injector for the Subcutaneous Self-injection of Bimekizumab Solution by Subjects With Active Psoriatic Arthritis
NCT04242446PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa
NCT04242498PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa
NCT05020249PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Korean Study Participants With Moderate to Severe Plaque Psoriasis
NCT06011733PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Bimekizumab in Chinese Adult Study Participants With Moderate to Severe Plaque Psoriasis
NCT06742333PHASE2RECRUITINGEarly Intervention in Plaque Psoriasis: is Bimekizumab Able to Delay Chronic Inflammation?
NCT07138898PHASE2NOT_YET_RECRUITINGImmunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty
NCT02430909PHASE2COMPLETEDMultiple Dose Study of UCB4940 as add-on to Certolizumab Pegol in Subjects With Rheumatoid Arthritis
NCT02905006PHASE2COMPLETEDStudy to Evaluate Safety and Efficacy of Different Doses of Bimekizumab in Patients With Chronic Plaque Psoriasis
NCT02963506PHASE2COMPLETEDA Study to Evaluate the Efficacy and Safety of Different Doses of Bimekizumab in Subjects With Active Ankylosing Spondylitis
NCT02969525PHASE2COMPLETEDA Study to Evaluate the Dose Response Based on the Efficacy, Safety and Tolerability of Bimekizumab in Subjects With Active Psoriatic Arthritis Which is a Type of Inflammatory Arthritis
NCT03010527PHASE2COMPLETEDA Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Patients With Chronic Plaque Psoriasis
NCT03025542PHASE2COMPLETEDA Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), and Safety of Bimekizumab in Patients With Chronic Plaque Psoriasis
NCT03215277PHASE2COMPLETEDA Study to Test the Efficacy and Safety of Bimekizumab and Certolizumab Pegol in Patients With Active Ankylosing Spondylitis
NCT03230292PHASE2COMPLETEDA Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Adult Patients With Chronic Plaque Psoriasis
NCT03248531PHASE2COMPLETEDA Study to Test the Efficacy, Safety and Pharmacokinetics of Bimekizumab in Subjects With Moderate to Severe Hidradenitis Suppurativa.

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).