Levilimab

drug
On this page

Also known as Bcd-089

Summary

Levilimab (CHEMBL4650406) is a phase-3 clinical-stage antibody (ATC L04AC25); indicated across 3 conditions including rheumatoid arthritis and severe acute respiratory syndrome.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • ATC class: L04AC25
  • Indications: 3 conditions
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650406
NameLevilimab
TypeAntibody
Max phase3
ATCL04AC25

Also known as: Bcd-089, BCD-089, Levilimab, LEVILIMAB

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

3 indications (0 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
rheumatoid arthritis3MONDO:0008383EFO:0000685
severe acute respiratory syndrome3MONDO:0005091MONDO:0100096
immune system disorder3MONDO:0005046EFO:0000540

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE33
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05800327PHASE3ACTIVE_NOT_RECRUITINGA Two-Stage Study of the Efficacy, Safety, Pharmacokinetics, Pharmacodynamics and Immunogenicity of Various Doses of Levilimab When Administered Intravenously and Subcutaneously to Healthy Subjects and Subjects With Active Rheumatoid Arthritis
NCT04227366PHASE3COMPLETEDStudy of the Efficacy and Safety of BCD-089 in Combination With Methotrexate in Patients With Active Rheumatoid Arthritis
NCT04397562PHASE3COMPLETEDA Clinical Trial of the Efficacy and Safety of Levilimab (BCD-089) in Patients With Severe COVID-19
NCT03103438PHASE1COMPLETEDFirst-in-human Study of Safety, Pharmacokinetics and Pharmacodynamics of Various Doses of BCD-089 in Healthy Subjects

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).