Nedosiran Sodium

drug
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Also known as Dcr-phxcRivfloza

Summary

Nedosiran Sodium (CHEMBL4594338) is an approved oligonucleotide; indicated across 2 conditions including primary hyperoxaluria.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Oligonucleotide
  • Indications: 2 conditions
  • Clinical trials: 5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4594338
NameNedosiran Sodium
TypeOligonucleotide
Max phase4

Also known as: Dcr-phxc, DCR-PHXC, Nedosiran sodium, Rivfloza, NEDOSIRAN SODIUM

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 (2 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
primary hyperoxaluria4MONDO:0002474MONDO:0002474

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

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
PHASE22
PHASE12
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04042402PHASE3ACTIVE_NOT_RECRUITINGLong Term Extension Study in Patients With Primary Hyperoxaluria
NCT04580420PHASE2RECRUITINGSafety & Efficacy of DCR-PHXC in Patients With PH1 and ESRD
NCT03847909PHASE2COMPLETEDA Study to Evaluate DCR-PHXC in Children and Adults With Primary Hyperoxaluria Type 1 and Primary Hyperoxaluria Type 2
NCT03392896PHASE1COMPLETEDStudy of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria
NCT04555486PHASE1COMPLETEDStudy to Evaluate Safety, Tolerability, PK and PD of DCR-PHXC in PH Type 3 Patients

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).