Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases : A Phase 2, Open-Label, Single-Arm, Cohort Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sparsentan Treatment in Pediatric Subjects With Selected Proteinuric Glomerular Diseases
This is a multicenter, open-label, 112-week study of sparsentan in approximately 57 pediatric subjects aged ≥1 year to <18 years with selected proteinuric glomerular diseases, divided into 2 populations, defined as follows:Population 1: Subjects with selected proteinuric glomerular diseases associated with Focal Segmental Glomerulosclerosis (FSGS) and Minimal Change Disease (MCD) histological patternsPopulation 2: Subjects with kidney biopsy-confirmed immunoglobulin A nephropathy (IgAN), immunoglobulin A vasculitis (IgAV), or subjects with Alport syndrome (AS)The study will evaluate long-term safety, tolerability, and efficacy with pharmacokinetic evaluations at Day 1 (Baseline), Day 2 (Visit 4), and Week 12 (Visit 9). For each population, subjects will be enrolled in 3 cohorts based on age ranges.Study Enrollment:Population 1: FSGS and/or MCD (30 subjects total)Cohort 1 (6 subjects): ≥8 years to <18 yearsCohort 2 (18 subjects): ≥3 years to <8 yearsCohort 3 (6 subjects): ≥1 year to <3 yearsPopulation 2: IgAN, IgAV, or AS (27 subjects total)Cohort 1 (9 subjects): ≥8 years to <18 yearsCohort 2 (12 subjects): ≥5 years to <8 yearsCohort 3 (6 subjects): ≥2 years to <5 years.
Medienart: |
Klinische Studie |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
ClinicalTrials.gov - (2023) vom: 14. Dez. Zur Gesamtaufnahme - year:2023 |
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Sprache: |
Englisch |
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Links: |
Volltext [kostenfrei] |
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Anmerkungen: |
Source: Link to the current ClinicalTrials.gov record., First posted: August 13, 2021, Last downloaded: ClinicalTrials.gov processed this data on December 20, 2023, Last updated: December 20, 2023 |
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Study ID: |
NCT05003986 |
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Veröffentlichungen zur Studie: |
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fisyears: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
CTG00780234X |
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245 | 1 | 0 | |a Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases |b A Phase 2, Open-Label, Single-Arm, Cohort Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sparsentan Treatment in Pediatric Subjects With Selected Proteinuric Glomerular Diseases |
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520 | |a This is a multicenter, open-label, 112-week study of sparsentan in approximately 57 pediatric subjects aged ≥1 year to <18 years with selected proteinuric glomerular diseases, divided into 2 populations, defined as follows:Population 1: Subjects with selected proteinuric glomerular diseases associated with Focal Segmental Glomerulosclerosis (FSGS) and Minimal Change Disease (MCD) histological patternsPopulation 2: Subjects with kidney biopsy-confirmed immunoglobulin A nephropathy (IgAN), immunoglobulin A vasculitis (IgAV), or subjects with Alport syndrome (AS)The study will evaluate long-term safety, tolerability, and efficacy with pharmacokinetic evaluations at Day 1 (Baseline), Day 2 (Visit 4), and Week 12 (Visit 9). For each population, subjects will be enrolled in 3 cohorts based on age ranges.Study Enrollment:Population 1: FSGS and/or MCD (30 subjects total)Cohort 1 (6 subjects): ≥8 years to <18 yearsCohort 2 (18 subjects): ≥3 years to <8 yearsCohort 3 (6 subjects): ≥1 year to <3 yearsPopulation 2: IgAN, IgAV, or AS (27 subjects total)Cohort 1 (9 subjects): ≥8 years to <18 yearsCohort 2 (12 subjects): ≥5 years to <8 yearsCohort 3 (6 subjects): ≥2 years to <5 years | ||
650 | 2 | |a Glomerulosclerosis, Focal Segmental | |
650 | 2 | |a Nephritis, Hereditary | |
650 | 2 | |a Glomerulonephritis, IGA | |
650 | 2 | |a Nephrosis, Lipoid | |
650 | 2 | |a Vasculitis | |
650 | 2 | |a IgA Vasculitis | |
650 | 4 | |a Study Type: Interventional | |
650 | 4 | |a Recruitment Status: Recruiting | |
650 | 4 | |a Phase: Phase 2 | |
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