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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.
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:
This is a non-interventional study that will last up to 2 years.
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| Measure | Description | Time Frame |
|---|---|---|
| Collect stone formation data in PH3 patients | Collect data on the rate of new stone formation in PH3 patients of at least 2 years of age | Assess participants' stone formation rates over the course of 2 years |
| Assess relationship between urine oxalate (Uox) levels and stone formations in PH3 patients | Explore the potential relationship between Uox levels and new stone formation in patients (≥ 2 years of age) with genetically confirmed PH3 and relatively intact renal function | Measure participants' Uox levels over the course of 2 years |
| Collect data on the degree of nephrocalcinosis in PH3 patients | Collect data on the degree of nephrocalcinosis in PH3 patients of at least 2 years of age | Assess the change in nephrocalcinosis grade over the course of 2 years |
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Key inclusion criteria
Genetically confirmed PH3
For participants at least 2 years of age, history of stone events (defined as presence of calcifications in the urinary tract and/or kidney, their relative location, and the number and size of stones) during the last 3 years and/or presence of pre-existing stones detected by renal ultrasound at Screening
Uox ≥ 0.7 mmol/24 hours (adjusted per 1.73 m2 BSA in participants < 18 years of age) OR if not able to collect 24-hour urine, average spot Uox to creatinine ratio at Screening above the 95th percentile for age:
eGFR at Screening ≥ 30 mL/min or for infants aged less than 12 months, serum creatinine below the 97th percentile of a healthy population
Key Exclusion Criteria:
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This is a natural history study in adults, adolescents, and children (starting from birth) with genetically confirmed PH3 who have a history of stone events during the last 3 years and/or the presence of preexisting stones detected by renal ultrasounds at Screening, and an eGFR > 30 mL/min/1.73 m2 or serum creatinine below the 97th percentile for patients younger than 12 months old.
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| Name | Affiliation | Role |
|---|---|---|
| Verity Rawson | Dicerna, A Novo Nordisk Company | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clinical Trial Site | Boston | Massachusetts | 02115 | United States | ||
| Clinical Trial Site |
| ID | Term |
|---|---|
| D006960 | Hyperoxaluria, Primary |
| D007669 | Kidney Calculi |
| D009397 | Nephrocalcinosis |
| ID | Term |
|---|---|
| D006959 | Hyperoxaluria |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| New York |
| New York |
| 10016 |
| United States |
| Clinical Trial Site | Toronto | Ontario | M5G 1X8 | Canada |
| Clinical Trial Site | Heidelberg | 69120 | Germany |
| Clinical Trial Site | Warsaw | 04-141 | Poland |
| Clinical Trial Site | London | WC1N 3JH | United Kingdom |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D002239 | Carbohydrate Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D053040 | Nephrolithiasis |
| D052878 | Urolithiasis |
| D014545 | Urinary Calculi |
| D002137 | Calculi |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D002114 | Calcinosis |
| D002128 | Calcium Metabolism Disorders |