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Clinical Trial Summary

A phase 1 study of DCR-PH1 in patients with primary hyperoxaluria type 1 (PH1) to determine the safety, tolerability, pharmacokinetic (PK) and pharmacodynamics (PD) effects of DCR-PH1 administered via-intravenous infusion (IV)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02795325
Study type Interventional
Source Dicerna Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 1
Start date May 13, 2016
Completion date October 14, 2016

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT03655223 - Early Check: Expanded Screening in Newborns
Completed NCT02830009 - IDENTIFICATION OF A MULTI-ANALYTE PROFILE FOR PRIMARY HYPEROXALURIA AND COMPARISON WITH HEALTHY SIBLINGS AND IDIOPATHIC HYPERCALCIURIA N/A
Completed NCT03067142 - Proteomics of Primary Hyperoxaluria Type 1
Active, not recruiting NCT04152200 - A Study to Evaluate Lumasiran in Patients With Advanced Primary Hyperoxaluria Type 1 Phase 3
Recruiting NCT05001269 - Nedosiran in Pediatric Patients From Birth to 11 Years of Age With PH and Relatively Intact Renal Function Phase 2
Recruiting NCT04982393 - BONAPH1DE, A Prospective Observational Study of Patients With Primary Hyperoxaluria Type 1 (PH1)
Recruiting NCT04580420 - Safety & Efficacy of DCR-PHXC in Patients With PH1/2 and ESRD Phase 2