Pembrolizumab products (Keytruda, Keytruda Qlex) (New)
Summary
Humana Indiana Medicaid has established a new prior authorization policy effective November 1, 2026, for pembrolizumab products (Keytruda intravenous powder, Keytruda intravenous solution, and Keytruda Qlex subcutaneous solution) covering 26 cancer indications. The policy specifies clinical criteria, exclusions (including prior anti-PD-1/PD-L1 therapy), and approval durations of 6 months or as determined through clinical review for each indication. Billing teams must obtain prior authorization before these drugs are dispensed or claims will be denied.
Get alerts when payers change rules like this one
We check Humana and other payers every day and email you when a change matches your specialty and state.