Nedosiran Sodium
drugOn this page
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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4594338 |
| Name | Nedosiran Sodium |
| Type | Oligonucleotide |
| Max phase | 4 |
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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| primary hyperoxaluria | 4 | MONDO:0002474 | MONDO: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
| Phase | Trials |
|---|---|
| PHASE2 | 2 |
| PHASE1 | 2 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04042402 | PHASE3 | ACTIVE_NOT_RECRUITING | Long Term Extension Study in Patients With Primary Hyperoxaluria |
| NCT04580420 | PHASE2 | RECRUITING | Safety & Efficacy of DCR-PHXC in Patients With PH1 and ESRD |
| NCT03847909 | PHASE2 | COMPLETED | A Study to Evaluate DCR-PHXC in Children and Adults With Primary Hyperoxaluria Type 1 and Primary Hyperoxaluria Type 2 |
| NCT03392896 | PHASE1 | COMPLETED | Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria |
| NCT04555486 | PHASE1 | COMPLETED | Study 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: primary hyperoxaluria