Depemokimab

drug
On this page

Also known as AQ-82742999AQ82742999GSK-3511294Gsk3511294

Summary

Depemokimab (CHEMBL4650469) is a phase-3 clinical-stage antibody; indicated across 4 conditions including granulomatosis with polyangiitis and nasal cavity polyp.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 4 conditions
  • Clinical trials: 16

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650469
NameDepemokimab
TypeAntibody
Max phase3

Also known as: AQ-82742999, AQ82742999, Depemokimab, GSK-3511294, Gsk3511294, GSK3511294, DEPEMOKIMAB

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 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
granulomatosis with polyangiitis3MONDO:0012105EFO:0005297
nasal cavity polyp3MONDO:0006314EFO:1000391
hypereosinophilic syndrome3MONDO:0015691EFO:1001467
asthma3MONDO:0004979MONDO:0004979

Clinical trials

Total trials: 16.

Phase distribution

PhaseTrials
PHASE313
PHASE13

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05263934PHASE3ACTIVE_NOT_RECRUITINGEfficacy and Safety of Depemokimab Compared With Mepolizumab in Adults With Relapsing or Refractory Eosinophilic Granulomatosis With Polyangiitis (EGPA)
NCT05334368PHASE3RECRUITINGDepemokimab in Participants With Hypereosinophilic Syndrome, Efficacy, and Safety Trial
NCT06959095PHASE3RECRUITINGDepemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA -1)
NCT06961214PHASE3RECRUITINGDepemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA-2)
NCT06979323PHASE3RECRUITINGDepemokimab Asthma Imaging and Bronchoscopy Sub-Study
NCT07177339PHASE3RECRUITINGeValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation
NCT07456033PHASE3NOT_YET_RECRUITINGA Study of Efficacy and Safety of Depemokimab Compared With Placebo in Adults and Adolescents With at Risk Type 2 Asthma
NCT04718103PHASE3COMPLETEDA Study of GSK3511294 (Depemokimab) in Participants With Severe Asthma With an Eosinophilic Phenotype
NCT04718389PHASE3COMPLETEDA Study of GSK3511294 (Depemokimab) Compared With Mepolizumab or Benralizumab in Participants With Severe Asthma With an Eosinophilic Phenotype
NCT04719832PHASE3COMPLETEDPlacebo-controlled Efficacy and Safety Study of GSK3511294 (Depemokimab) in Participants With Severe Asthma With an Eosinophilic Phenotype
NCT05243680PHASE3COMPLETEDAn Open-Label Extension Study of GSK3511294 (Depemokimab) in Participants Who Were Previously Enrolled in 206713 (NCT04719832) or 213744 (NCT04718103)
NCT05274750PHASE3COMPLETEDEfficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal Polyps
NCT05281523PHASE3COMPLETEDEfficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal Polyps (ANCHOR-2)
NCT03287310PHASE1COMPLETEDFirst Time in Human (FTIH) Study to Evaluate Safety, Tolerability, Immunogenicity, Pharmacokinetics (PK) and Pharmacodynamics (PD) of GSK3511294 Administered Subcutaneously (SC) in Subjects With Mild to Moderate Asthma
NCT05140200PHASE1COMPLETEDStudy of GSK3511294 in Healthy Chinese Participants
NCT05602025PHASE1COMPLETEDA Study to Compare the Pharmacokinetics (PK) of Depemokimab When Delivered With a Safety Syringe Device (SSD) or an Autoinjector in Healthy Adult Participants

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).