Edasalonexent

drug
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Also known as Cat 1004Cat-1004CAT1004Edasalonexento

Summary

Edasalonexent (CHEMBL3786673) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including duchenne muscular dystrophy and type 2 diabetes mellitus.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 2 conditions
  • Clinical trials: 5
  • Chemistry: 490.7 Da · C31H42N2O3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3786673
NameEdasalonexent
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID44626120
Molecular formulaC31H42N2O3
Molecular weight490.7
InChIKeyJQLBBYLGWHUHRW-KUBAVDMBSA-N

SMILES: CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)NCCNC(=O)C1=CC=CC=C1O

IUPAC name: N-[2-[[(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoyl]amino]ethyl]-2-hydroxybenzamide

Also known as: Cat 1004, CAT 1004, Cat-1004, CAT-1004, CAT1004, Edasalonexent, Edasalonexento, EDASALONEXENT

Patent coverage: 60 distinct patent families (178 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

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

2 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
Duchenne muscular dystrophy3MONDO:0010679MONDO:0010679
type 2 diabetes mellitus1MONDO:0005148MONDO:0005148

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
PHASE32
PHASE12
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03703882PHASE3COMPLETEDPhase III Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy
NCT03917719PHASE3TERMINATEDAn Open-Label Extension Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy
NCT02439216PHASE1/PHASE2COMPLETEDPhase 1/2 Study in Boys With Duchenne Muscular Dystrophy
NCT01511900PHASE1COMPLETEDA Multiple Ascending Dose Study of CAT-1004 in Patients With Type 2 Diabetes
NCT01670773PHASE1COMPLETEDA Study of CAT-1004 Biomarkers 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).