drugset / Trial / NCT04580420

Safety & Efficacy of DCR-PHXC in Patients With PH1 and ESRD

NCT04580420 ↗

Phase 2 Recruiting 28 enrolled Dicerna Pharmaceuticals, Inc.
NaSequentialOpen-labelTreatment

Summary

The aim of this study is to evaluate DCR-PHXC in participants with PH1 and severe renal impairment, with or without dialysis.

Timeline

Start
2021-04-15
Primary completion
2031-12-30
Completion
2032-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject DCR-PHXC Unknown — Subcutaneous