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Aimovig (Erenumab) & Signal Identification

    Basic Details
    Last Updated
    Thursday, October 12, 2023
    Original Posting Date
    Health Outcome(s)
    signal identification
    Signal Identification
    Meets requirements of FD&C Act Sec 505(o) prior to requiring a PMR
    Regulatory Determination / Use

    FDA initiated this pilot study in Sentinel to explore the use of TreeScanTM for routine drug safety surveillance, using a use case of Aimovig (erenumab). TreeScan is a signal identification approach that scans thousands of health outcomes simultaneously while adjusting for multiple scenarios that can be used to monitor the underlying assumption of no clinical differences.

    The study specifically sought to monitor non-pregnancy and non-cancer outcomes among new users of Aimovig using a self-controlled risk interval analysis and tree-based scan statistics. FDA determined the statistical alerts generated by the TreeScan analysis do not warrant further evaluation or action. This pilot demonstrated that tree-based scan statistics can be applied to the Sentinel Distributed Database (SDD) using a self-controlled risk interval design to simultaneously evaluate thousands of safety outcomes for medicines as an additional safety surveillance tool.