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The Gilenya Pregnancy Registry

    • Novartis Pharmaceuticals

    Project: Clinical Trial

    Project Details

    Description

    The purpose of the Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis (MS) is to continuously monitor, evaluate, and assess for major and minor teratogenic effects in the offspring of women exposed to fingolimod before (up to 8 weeks before last menstrual period (LMP) and during pregnancy in routine clinical practice. The overall aim is to collect and evaluate data on maternal, fetal, and infant outcomes and compare it with reference populations.
    StatusActive
    Effective start/end date15/10/112/01/31

    Collaborative partners

    Keywords

    • Pathologic Processes
    • Demyelinating Autoimmune Diseases, CNS
    • Autoimmune Diseases of the Nervous System
    • Nervous System Diseases
    • Demyelinating Diseases
    • Autoimmune Diseases
    • Immune System Diseases
    • Multiple Sclerosis
    • Sclerosis
    • Sphingosine 1 Phosphate Receptor Modulators
    • Molecular Mechanisms of Pharmacological Action
    • Immunosuppressive Agents
    • Immunologic Factors
    • Physiological Effects of Drugs
    • Fingolimod Hydrochloride
    • Fingolimod
    • FTY720
    • Gilenya
    • MS
    • Safety
    • Pregnancy
    • Pregnancy Outcomes

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