Ebdarokimab

drug
On this page

Also known as AK-101Ak101

Summary

Ebdarokimab (CHEMBL4650437) is a phase-3 clinical-stage antibody; indicated across 3 conditions including psoriasis and ulcerative colitis.

At a glance

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

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650437
NameEbdarokimab
TypeAntibody
Max phase3

Also known as: AK-101, Ak101, AK101, Ebdarokimab, EBDAROKIMAB

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
psoriasis3MONDO:0005083EFO:0000676
ulcerative colitis1MONDO:0005101EFO:0000729

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

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE31
PHASE1/PHASE21
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05120297PHASE3COMPLETEDA Phase 3 Study of Efficacy and Safety of AK101 in Subjects With Psoriasis
NCT04172233PHASE1/PHASE2COMPLETEDA Clinical Study of AK101 in Subjects With Moderate to Severe Plaque Psoriasis
NCT04173637PHASE2COMPLETEDClinical Study of AK101 in Subjects With Moderate to Severe Plaque Psoriasis
NCT06281704PHASE1COMPLETEDA Study of AK101 in Subjects With Moderately to Severely Active Ulcerative Colitis

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).