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Updated Prior Authorization Requirements for Treatment of hATTR Effective November 1, 2026

Texas Medicaid·TX · Internal Medicine, Neurology, Genetics·Prior Authorization
Effective date
Nov 1, 2026
We identified it
Oct 24, 2026
Days to comply
4 days

Summary

Effective November 1, 2026, Texas Medicaid introduces new prior authorization requirements for eplontersen (Wainua) treatment of hereditary transthyretin-mediated amyloidosis (hATTR) polyneuropathy, including mandatory vitamin A supplementation and therapy non-duplication rules. Existing prior authorization criteria for patisiran (Onpattro) and vutrisiran (Amvuttra) are updated to include eplontersen in non-duplication exclusions.

Action Required

Before Nov 1, 2026
By November 1, 2026: Billing and prior authorization teams must implement the following changes in the billing system and prior authorization workflows: (1) Configure procedure code C9311 (eplontersen/Wainua) to require prior authorization submission on the SMPA Request Form for Texas Medicaid; (2) Update prior authorization logic to enforce one 12-month approval duration per eplontersen request; (3) Implement screening criteria in the authorization system to verify client age (≥18 years), hATTR diagnosis (E851) with TTR mutation confirmation and clinical symptoms, vitamin A supplementation plan, and non-duplication against inotersen, patisiran, vutrisiran, and tafamidis meglumine; (4) Add eplontersen to existing non-duplication criteria for patisiran (Onpattro) and vutrisiran (Amvuttra) authorization checks; (5) For renewal requests, configure the system to verify prior treatment without adverse reaction and documented positive clinical response (neurologic improvement, motor function improvement, or disease progression slowing). Failure to implement prior authorization will result in claim denials. Contact TMHP Contact Center (800-925-9126) for clarification or MCO-specific administrative procedures.

Affected Billing Codes

C9311
E851