Pembrolizumab products (Keytruda, Keytruda Qlex) (New)
Summary
Humana Ohio Medicaid established a new prior authorization policy effective November 1, 2026, for pembrolizumab products (Keytruda intravenous powder, intravenous solution, and Keytruda Qlex subcutaneous solution) across 25 cancer indications. Each indication has specific clinical criteria, required combination or monotherapy regimens, biomarker requirements (CPS, PD-L1, dMMR/MSI-H, or TMB-high scores where applicable), and exclusions based on prior anti-PD-1/PD-L1 therapy. Initial and renewal approvals are granted for 6 months or as determined through clinical review.
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