K-877

drug
On this page

Summary

K-877 (CHEMBL3545412) is a phase-3 clinical-stage unknown; indicated across 6 conditions including hypertriglyceridemia and hyperlipidemia.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Indications: 6 conditions
  • Clinical trials: 14

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3545412
NameK-877
TypeUnknown
Max phase3

Also known as: K-877

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

6 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
hypertriglyceridemia3MONDO:0005347EFO:0004211
hyperlipidemia3MONDO:0021187MONDO:0021187
metabolic dysfunction-associated steatotic liver disease2MONDO:0013209EFO:0003095
metabolic dysfunction-associated steatohepatitis2MONDO:0007027EFO:1001249

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

Clinical trials

Total trials: 14.

Phase distribution

PhaseTrials
PHASE19
PHASE34
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03001817PHASE3COMPLETEDStudy to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Normal Renal Function
NCT03011450PHASE3COMPLETEDStudy to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Mild or Moderate Renal Impairment
NCT03071692PHASE3TERMINATEDPemafibrate to Reduce Cardiovascular OutcoMes by Reducing Triglycerides IN patiENts With diabeTes (PROMINENT)
NCT05923281PHASE3COMPLETEDA Phase III Confirmatory Study of K-877 (Pemafibrate) in Patients With Hypercholesterolemia and Statin Intolerance
NCT03350165PHASE2COMPLETEDA Study of Pemafibrate in Patients With Nonalcoholic Fatty Liver Disease (NAFLD)
NCT02273986PHASE1COMPLETEDDrug-Drug Interaction Study in Health Adult Volunteers
NCT02275962PHASE1COMPLETEDDrug-Drug Interaction Study in Healthy Adult Volunteers
NCT02275975PHASE1COMPLETEDDrug-Drug Interaction Study in Healthy Adult Volunteers
NCT02275988PHASE1COMPLETEDDrug-Drug Interaction Study in Healthy Adult Volunteers
NCT02276001PHASE1COMPLETEDDrug-Drug Interaction Study in Healthy Adult Volunteers
NCT02719431PHASE1COMPLETEDDrug-Drug Interaction Study to Assess the Effects of Multiple-Dose Administration of K-877 on the Pharmacodynamics and the Pharmacokinetics of Multiple-Dose Administration of Warfarin in Healthy Adult Volunteers
NCT02922465PHASE1COMPLETEDDrug-Drug Interaction Study to Assess the Effects of Multi Dose Clopidogrel on the Pharmacokinetics of Single-Dose K-877 in Healthy Adult Volunteers
NCT04237597PHASE1COMPLETEDPharmacokinetic Drug-Drug Interaction Study Between K-877 and CSG452 in Healthy Adult Volunteers
NCT04742218PHASE1COMPLETEDStudy to Assess the Food Effect of K-877 in Healthy Adult Volunteers

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).