Fruzaqla (fruquintinib)

Indications for Prior Authorization

Fruzaqla (fruquintinib)
  • For diagnosis of Metastatic colorectal cancer (mCRC)
    Indicated for the treatment of adult patients with metastatic colorectal cancer (mCRC) who have been previously treated with fluoropyrimidine , oxaliplatin, and irinotecan based chemotherapy, an anti VEGF therapy, and, if RAS wild type and medically appropriate, an anti-EGFR therapy

Criteria

Fruzaqla

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)
For diagnosis of Metastatic colorectal cancer (mCRC)

  • Diagnosis of metastatic colorectal cancer (mCRC)
  • AND
  • Patient has been previously treated with both of the following:
    • Fluoropyrimidine-, oxaliplatin-, irinotecan-based chemotherapy (e.g., FOLFOX, FOLFIRI, FOLFOXIRI)
    • Anti-VEGF biological therapy (e.g., Avastin [bevacizumab], Zaltrap [ziv-aflibercept])
    AND
  • One of the following:
    • Patient has RAS mutant tumors
    • OR
    • All of the following:
      • Patient has RAS wild-type tumors
      • AND
      • Patient has been previously treated with an anti-EGFR biological therapy (e.g., Vectibix [panitumumab], Erbitux [cetuximab])
      • AND
      • One of the following:
        • Trial and failure, contraindication or intolerance to Stivarga [regorafenib]
        • OR
        • For continuation of prior therapy
Fruzaqla

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)
For diagnosis of Metastatic colorectal cancer (mCRC)

  • Patient does not show evidence of progressive disease while on therapy
P & T Revisions

2024-05-13, 2024-01-08

  1. Fruzaqla Prescribing Information. Takeda Pharmaceuticals America, Inc., Lexington, MA. November 2023

  • 2024-05-13: Commercial formulary strategy to revise the embedded step to remove Lonsurf as a trial option.
  • 2024-01-08: New Program

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