Eribulin

Eribulin

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Eribulin mesylate was approved by the US FDA on November 15, 2010, to treat patients with metastatic breast cancer who have received at least two prior chemotherapy regimens for late-stage disease, including both anthracycline and taxane-based chemotherapies.

January 28, 2016: FDA approved Halaven (eribulin) for the treatment of liposarcoma that cannot be removed by surgery (unresectable) or is advanced/metastatic. this treatment is approved for patients who received prior chemotherapy that contained an anthracycline drug.

This drug should be coded