inotersen — United 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