Drugs / DCR-PHXC
Regulatory milestones approvals, filings & regulatory actions · 2 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansion | US (FDA) | RIVFLOZA | — | 2025-03-27 | fda.gov ↗ |
| Approved | US (FDA) | RIVFLOZA | — | 2023-09-29 | fda.gov ↗ |
Trials 7
Evidence & citations 5 cited values
Every value below carries the sentence it was read from. 8 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | DCR-PHXC | ClinicalTrials.gov intervention name — accepted as the source's own label NCT04042402 ↗ |
| Known as | Nedosiran | ClinicalTrials.gov intervention name — accepted as the source's own label NCT05993416 ↗ |
| Known as | Rivfloza | “Nedosiran (Rivfloza®) is an RNA interference (RNAi) therapy approved for individuals aged ≥ 2 years with primary hyperoxaluria type 1 (PH1)” PMID 40601241 ↗ Jul 2025 |
| Action | Inhibit | “Nedosiran silences lactate dehydrogenase (LDH) mRNA in hepatocytes, reducing oxalate levels.” PMID 40601241 ↗ Jul 2025 |
| Route | Subcutaneous | “DCR-PHXC is delivered via subcutaneous (SC) injection.” NCT03392896 ↗ |