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Outcome Monitoring Following Risankizumab Use: A Supplemental Signal Identification Analysis

    Basic Details
    Date Posted
    Status
    Complete
    Medical Product
    risankizumab
    Health Outcome(s)
    signal identification
    Description

    This analysis performed signal identification for risankizumab by monitoring non-pregnancy and non-cancer outcomes among new users of risankizumab compared to guselkumab in the Sentinel Distributed Database (SDD). We conducted this signal identification assessment using an active comparator design, the associated analysis used a self-controlled risk interval design. The study period includes data from April 23, 2019 through September 30, 2023. We distributed this request to 13 Sentinel Data Partners on March 11, 2024. The report includes data from six Sentinel Data Partners.

    Statistical alerts generated by this analysis do not on their own represent safety signals. Alerts are triaged in consideration of the study design, existing drug knowledge, therapeutic context, treated population, and potential public health impact. Alerts determined to be newly identified safety signals (NISS) follow the FDA’s Center for Drug Evaluation and Research manual of policies and procedures for NISS (MAPP 4121.3).

    The analytic package associated with this analysis can be found externally in Sentinel's Git Repository located here. The Git Repository serves as Sentinel's version control tracking system for analytic packages and technical documentation.

    Additional Details
    FDA Center
    CDER
    Time Period
    April 23, 2019 - September 30, 2023
    Analysis Type
    Signal Identification
    Population / Cohort
    Individuals 18 years of age and older
    Data Sources
    Sentinel Distributed Database (SDD)