Fruzaqla (fruquintinib)
Indications for Prior Authorization
Fruzaqla (fruquintinib)
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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])
- 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
References
- Fruzaqla Prescribing Information. Takeda Pharmaceuticals America, Inc., Lexington, MA. November 2023
Revision History
- 2024-05-13: Commercial formulary strategy to revise the embedded step to remove Lonsurf as a trial option.
- 2024-01-08: New Program