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A Study to Evaluate Lumasiran in Patients With Advanced Primary Hyperoxaluria Type 1

    • Alnylam Pharmaceuticals

    Project: Clinical Trial

    Project Details

    Description

    The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics (PK), and pharmacodynamics (PD) of lumasiran in patients with Advanced Primary Hyperoxaluria Type 1 (PH1).
    AcronymILLUMINATE-C
    StatusFinished
    Effective start/end date21/01/201/07/25

    Collaborative partners

    Keywords

    • PH1
    • Primary Hyperoxaluria
    • Hyperoxaluria
    • RNAi Therapeutic
    • siRNA
    • AGT
    • Systemic Oxalosis
    • Kidney Diseases
    • Urologic Diseases
    • Female Urogenital Diseases
    • Female Urogenital Diseases and Pregnancy Complications
    • Urogenital Diseases
    • Male Urogenital Diseases
    • Carbohydrate Metabolism Inborn Errors
    • Metabolism Inborn Errors
    • Inborn Genetic Diseases
    • Metabolic Diseases
    • Renal Agents
    • Lumasiran

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