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    1. Documents
    2. doc:fda:truseltiq

    Truseltiq (infigratinib) [package insert]. FDA.

    Regulatory approval published by the Food and Drug Administration.

    Citation

    QED Therapeutics, Inc. Truseltiq (infigratinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214622s000lbl.pdf. Revised May 2021. Accessed October 30, 2024.

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    Regulatory approvals

    Approved indications from this document for cancer drugs containing at least one biomarker.

    Indication Statements
    TRUSELTIQ is a kinase inhibitor indicated for the treatment of adults with previously treated, unresectable locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion or other rearrangement as detected by an FDA-approved test. This indication is approved under accelerated approval based on overall response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trial(s). 1

    Therapeutic response

    Precision oncology relationships for therapeutic response derived from this document.

    Organizations
    Biomarkers
    Cancer types
    Therapies
    Organizations Biomarkers Cancer types Therapies
    FDA (1) FGFR2::v Cholangiocarcinoma Infigratinib

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