Olpasiran

drug
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Also known as Amg 890AMG-890

Summary

Olpasiran (CHEMBL4650413) is a phase-3 clinical-stage oligonucleotide; indicated across 4 conditions including cardiovascular disorder and liver disorder.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Oligonucleotide
  • Indications: 4 conditions
  • Clinical trials: 9

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650413
NameOlpasiran
TypeOligonucleotide
Max phase3

Also known as: Amg 890, AMG 890, AMG-890, Olpasiran, OLPASIRAN

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
cardiovascular disorder3MONDO:0004995EFO:0000319
liver disorder1MONDO:0005154EFO:0001421
kidney disorder1MONDO:0005240EFO:0003086
atherosclerosis1MONDO:0005311EFO:0003914

Clinical trials

Total trials: 9.

Phase distribution

PhaseTrials
PHASE14
PHASE33
PHASE21
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05581303PHASE3ACTIVE_NOT_RECRUITINGOlpasiran Trials of Cardiovascular Events and Lipoprotein(a) Reduction (OCEAN(a)) - Outcomes Trial
NCT07136012PHASE3RECRUITINGOCEAN(a)-PreEvent - Olpasiran Trials of Cardiovascular Events And LipoproteiN(a) Reduction to Prevent First Major Cardiovascular Events
NCT07293260PHASE3RECRUITINGOlpasiran Trials of Cardiovascular Events and Lipoprotein(a) Reduction - Coronary Computed Tomography Angiography Trial
NCT04270760PHASE2COMPLETEDOlpasiran Trials of Cardiovascular Events And LipoproteiN(a) Reduction - DOSE Finding Study
NCT04987320PHASE1COMPLETEDA Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Olpasiran in Chinese Participants With Elevated Serum Lipoprotein(a)
NCT05481411PHASE1COMPLETEDA Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Olpasiran in Participants With Various Degrees of Hepatic Impairment
NCT05489614PHASE1COMPLETEDA Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Olpasiran in Participants With Normal Renal Function and Participants With Various Degrees of Renal Impairment
NCT06411860PHASE1COMPLETEDA Study to Assess the Effect of Olpasiran on QT/QTc Intervals in Healthy Participants
NCT07079267Not specifiedAVAILABLEOlpasiran Expanded Access Program

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).