Elobixibat

drug
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Also known as A-3309A3309AZD-7806AZD7806

Summary

Elobixibat (CHEMBL3039515) is a phase-3 clinical-stage small molecule (ATC A06AX09) targeting SLC10A2; indicated across 3 conditions including constipation disorder and metabolic dysfunction-associated steatohepatitis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: A06AX09
  • Targets: 1 (SLC10A2)
  • Indications: 3 conditions
  • Clinical trials: 11
  • Chemistry: 695.9 Da · C36H45N3O7S2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3039515
NameElobixibat
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID9939892
ATCA06AX09
Molecular formulaC36H45N3O7S2
Molecular weight695.9
InChIKeyXFLQIRAKKLNXRQ-UUWRZZSWSA-N

SMILES: CCCCC1(CN(C2=CC(=C(C=C2S(=O)(=O)C1)OCC(=O)N[C@H](C3=CC=CC=C3)C(=O)NCC(=O)O)SC)C4=CC=CC=C4)CCCC

IUPAC name: 2-[[(2R)-2-[[2-[(3,3-dibutyl-7-methylsulfanyl-1,1-dioxo-5-phenyl-2,4-dihydro-1lambda6,5-benzothiazepin-8-yl)oxy]acetyl]amino]-2-phenylacetyl]amino]acetic acid

Also known as: A-3309, A3309, AZD-7806, AZD7806, Elobixibat, ELOBIXIBAT

Patent coverage: 242 distinct patent families (780 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 779 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
SLC10A2Sodium/bile acid and sulphated solute cotransporter 2Inhibition8.920%Q12908

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Bile acid receptor.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
NR1H48.92IC501.2nMCHEMBL_ACT_26686529

Target pathways

Aggregated over 1 target gene(s): SLC10A2.

Top Reactome pathways

1 total, by targets touching each:

PathwayTargetsGenes
Recycling of bile acids and salts1SLC10A2

Dominant GO biological processes

GO termTargets
response to bacterium1
bile acid and bile salt transport1
monoatomic ion transport1
sodium ion transport1
lipid transport1
transmembrane transport1

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
constipation disorder3MONDO:0002203HP:0002019
metabolic dysfunction-associated steatohepatitis2MONDO:0007027EFO:1001249

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

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE25
PHASE43
PHASE33

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04784780PHASE4UNKNOWNLong-term Elobixibat for Chronic Constipation
NCT05165199PHASE4UNKNOWNElobixibat for Chronic Constipation Without Defecation Desire
NCT05703464PHASE4TERMINATEDElobixibat for Chronic Constipation Without Defecation Desire
NCT01827592PHASE3TERMINATED26 Week Efficacy and Safety Trial for Patients With Chronic Idiopathic Constipation
NCT01833065PHASE3TERMINATEDEfficacy and Safety Trial of Elobixibat in Patients With Chronic Idiopathic Constipation
NCT01895543PHASE3COMPLETEDSafety and Tolerability Extension Trial for Patients With Chronic Idiopathic Constipation
NCT01007123PHASE2COMPLETEDStudy of Elobixibat (A3309) in Patients With Chronic Idiopathic Constipation
NCT01038687PHASE2COMPLETEDEffect of Ileal Bile Acid Transporter Inhibitor in Functional Constipation
NCT01069783PHASE2COMPLETEDStudy of A3309 in Patients With Dyslipidemia
NCT02392546PHASE2WITHDRAWNElobixibat Colonic Motor Function Study
NCT04006145PHASE2COMPLETEDA Phase 2 Study of Elobixibat in Adults With NAFLD or NASH

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

9 molecules share ≥1 primary target. Top 9 by shared-target count:

MoleculeSourceStatusShared targets
CHENODIOLChEMBL + PubChemPhase 4 (approved)SLC10A2
CYCLOSPORINEChEMBL + PubChemPhase 4 (approved)SLC10A2
DEOXYCHOLIC ACIDChEMBL + PubChemPhase 4 (approved)SLC10A2
MARALIXIBATChEMBL + PubChemPhase 4 (approved)SLC10A2
MARALIXIBAT CHLORIDEChEMBL + PubChemPhase 4 (approved)SLC10A2
URSODIOLChEMBL + PubChemPhase 4 (approved)SLC10A2
TAURURSODIOLChEMBLPhase 4 (approved)SLC10A2
LINERIXIBATChEMBLPhase 3SLC10A2
TAURODEOXYCHOLIC ACIDChEMBLPhase 2SLC10A2