Lumasiran for Advanced Primary Hyperoxaluria Type 1: Phase 3 ILLUMINATE-C Trial.

American journal of kidney diseases : the official journal of the National Kidney Foundation(2022)

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摘要
Primary hyperoxaluria type 1 (PH1) is a rare genetic disease characterized by excessive hepatic oxalate production that frequently causes kidney failure. Lumasiran is an RNA interference therapeutic that is administered subcutaneously for the treatment of PH1. Lumasiran has been shown to reduce oxalate levels in the urine and plasma of patients with PH1 who have relatively preserved kidney function. In the ILLUMINATE-C study, the efficacy and safety of lumasiran were evaluated in patients with PH1 and advanced kidney disease, including a cohort of patients undergoing hemodialysis. During the 6-month primary analysis period, lumasiran resulted in substantial reductions in plasma oxalate with acceptable safety in patients with PH1 complicated by advanced kidney disease.
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关键词
Lumasiran,RNA interference (RNAi),adverse events,anti-drug antibodies,cardiac dysfunction,efficacy,glycolate,hemodialysis,kidney disease,nephrocalcinosis,pediatric,pharmacodynamics,pharmacokinetics,phase 3 clinical trial,plasma oxalate (POx),primary hyperoxaluria type 1 (PH1),safety,systemic oxalosis,urinary oxalate (UOx)
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