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Clinical Trial Summary

This is a natural history study of adults, adolescents, and children (starting at birth) with genetically confirmed primary hyperoxaluria type 3 (PH3) who have a history of stone events during the last 3 years and/or the presence of pre existing stones detected by renal ultrasound at screening.


Clinical Trial Description

The relationship between the level of Uox and the incidence of kidney stones and/or nephrocalcinosis in patients with PH3 has not been established. The goal of this study is to record 24-hour Uox levels and the incidence of new stone formation and/or the degree of nephrocalcinosis in patients with PH3 over time. Potential participants are screened over an up-to-7 week period according to the eligibility criteria and will then be followed every 6 months over an up-to-2-year period to determine the annualized new stone formation rate (number of new stones being formed per year) and the change in the degree of nephrocalcinosis (if applicable). New stone formation is defined as occurrence of any of the following: - Spontaneous stone passage in the absence of pre-existing stones - Stone passage occurring without change in the number of pre-existing stones detected by renal ultrasound - Appearance of new stones on renal ultrasound or 100% or more growth of a pre-existing stone (estimated area) - Surgical removal of newly formed stones Note: Spontaneous passage or surgical removal of pre-existing stones does not meet the criteria for new stone formation. This is a non-interventional study that will last up to 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04542590
Study type Observational [Patient Registry]
Source Dicerna Pharmaceuticals, Inc., a Novo Nordisk company
Contact
Status Active, not recruiting
Phase
Start date September 9, 2021
Completion date August 5, 2024

See also
  Status Clinical Trial Phase
Completed NCT04555486 - Study to Evaluate Safety, Tolerability, PK and PD of DCR-PHXC in PH Type 3 Patients Phase 1
Enrolling by invitation NCT03655223 - Early Check: Expanded Screening in Newborns
Recruiting NCT05001269 - Nedosiran in Pediatric Patients From Birth to 11 Years of Age With PH and Relatively Intact Renal Function Phase 2
Not yet recruiting NCT06465472 - Evaluation of the Efficacy and Safety of Stiripentol in Patients 6 Years and Older With Primary Hyperoxaluria Type 1, 2 or 3 Phase 3