Summary
Humana Medicare Advantage updated its Rituximab Products prior authorization policy effective January 1, 2023, with a revision date of June 24, 2026. The policy establishes step-therapy requirements for branded rituximab products (Rituxan, Truxima) across nine covered indications, requiring documented intolerance or contraindication to biosimilars (Ruxience, Riabni) before approval, with exceptions for continuation of prior therapy within 365 days. Key exclusions include high-dose CLL therapies and maintenance therapy duration limits (2 years for CLL and low-grade NHL).
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