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inotersenUnited Healthcare

hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy

Initial criteria

  • Diagnosis of hATTR amyloidosis with polyneuropathy
  • Patient has a pathogenic TTR mutation (e.g., V30M)
  • Patient is not receiving Tegsedi in combination with either of the following: (a) Oligonucleotide agents [e.g., Onpattro (patisiran), Amvuttra (vutrisiran)] (b) Tafamidis (e.g., Vyndaqel, Vyndamax)

Reauthorization criteria

  • Documentation of positive clinical response to Tegsedi therapy
  • Patient is not receiving Tegsedi in combination with either of the following: (a) Oligonucleotide agents [e.g., Onpattro (patisiran), Amvuttra (vutrisiran)] (b) Tafamidis (e.g., Vyndaqel, Vyndamax)

Approval duration

12 months