Lutikizumab

drug
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Also known as A-1234138Abt-981

Summary

Lutikizumab (CHEMBL4594518) is a phase-3 clinical-stage antibody; indicated across 4 conditions including hidradenitis suppurativa and osteoarthritis, knee.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 4 conditions
  • Clinical trials: 11

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4594518
NameLutikizumab
TypeAntibody
Max phase3

Also known as: A-1234138, Abt-981, ABT-981, Lutikizumab, LUTIKIZUMAB

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

4 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
hidradenitis suppurativa3MONDO:0006559EFO:1000710
osteoarthritis, knee2MONDO:0005416EFO:0004616
ulcerative colitis2MONDO:0005101EFO:0000729
osteoarthritis1MONDO:0005178MONDO:0005178

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE29
PHASE31
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06468228PHASE3ACTIVE_NOT_RECRUITINGA Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa
NCT05139602PHASE2ACTIVE_NOT_RECRUITINGA Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are Naïve to Biologic Therapy
NCT06257875PHASE2ACTIVE_NOT_RECRUITINGA Study to Assess Adverse Events and Change in Disease Activity From Intravenous (IV) and Subcutaneous (SC) Lutikizumab in Adult Participants With Active Ulcerative Colitis
NCT06524635PHASE2RECRUITINGA Study to Assess Molecular Changes in Adult Participants With Moderate to Severe Hidradenitis Suppurativa or With Moderate to Severe Atopic Dermatitis Receiving Subcutaneous Injections of Lutikizumab
NCT06548542PHASE2RECRUITINGStudy of Targeted Therapies for the Treatment of Adult Participants With Moderate to Severe Crohn’s Disease
NCT06718101PHASE2ACTIVE_NOT_RECRUITINGA Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or in Combination, for the Treatment of Moderate to Severe Atopic Dermatitis
NCT06865105PHASE2RECRUITINGStudy of Targeted Therapies for the Treatment of Adult Participants With Active Psoriatic Arthritis
NCT06972446PHASE2RECRUITINGA Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid Arthritis
NCT02087904PHASE2COMPLETEDA Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981 in Patients With Knee Osteoarthritis
NCT02384538PHASE2COMPLETEDA Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With Erosive Hand Osteoarthritis
NCT01668511PHASE1COMPLETEDA Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple Subcutaneous Injections of ABT-981 in Patients With Osteoarthritis of the Knee

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).