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Retevmo® (selpercatinib) – Expanded indications

May 29, 2024 - The FDA approved Eli Lilly’s Retevmo (selpercatinib), for the treatment of adult and pediatric patients 2 years of age and older with Advanced or metastatic medullary thyroid cancer with a RET mutation, as detected by an FDA-approved test, who require systemic therapy. Advanced or metastatic thyroid cancer with a RET gene fusion, as detected by an FDA-approved test, who require systemic therapy and who are radioactive iodine-refractory (if radioactive iodine is appropriate); Locally advanced or metastatic solid tumors with a RET gene fusion, as detected by an FDA-approved test, that have progressed on or following prior systemic treatment or who have no satisfactory alternative treatment options.

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