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The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics (PK), and pharmacodynamics (PD) of lumasiran in infants and young children with confirmed primary hyperoxaluria type 1 (...
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Lead Sponsor
Alnylam Pharmaceuticals
NCT04580420 · Primary Hyperoxaluria Type 1, End Stage Renal Disease
NCT00588562 · Primary Hyperoxaluria, Dent Disease, and more
NCT06065852 · Adenine Phosphoribosyltransferase Deficiency, AH Amyloidosis, and more
NCT05843851 · Cystinosis, Primary Hyperoxaluria
NCT05993416 · Primary Hyperoxaluria Type 1 (PH1)
Clinical Trial Site
Rochester, Minnesota
Clinical Trial Site
Houston, Texas
Clinical Trial Site
Lyon
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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