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Medicare AdvantagePrior AuthMedium impact

Motpoly XR (lacosamide extended release) (Revised)

Humana·Neurology, Pediatrics·Medicare Advantage
Effective date
Aug 27, 2025
We identified it
Jun 25, 2026
Days to comply

Summary

Humana Medicare Advantage updated the Motpoly XR (lacosamide extended-release) prior authorization policy effective August 27, 2025. The policy requires prior authorization for seizure treatment with specific clinical criteria: patients must have documented failure with generic lacosamide AND at least one other antiepileptic drug, weigh at least 50 kg, and meet diagnosis requirements for either partial-onset seizures or adjunctive generalized tonic-clonic seizure treatment.

Action Required

Action needed
By August 27, 2025: Billing and prior authorization teams must implement this new Motpoly XR prior authorization requirement in the billing system. Specifically: (1) Configure system to require prior authorization for all Motpoly XR pharmacy claims under Medicare Advantage; (2) Update prior auth submission templates to capture required clinical documentation including diagnosis (partial-onset seizures OR generalized tonic-clonic seizures), patient weight (must be ≥50 kg), and evidence of prior treatment failure with generic lacosamide AND at least one other specified antiepileptic drug (levetiracetam, lamotrigine, carbamazepine, zonisamide, divalproex, gabapentin, or topiramate); (3) Notify providers and patient care coordinators of the updated criteria; (4) Train staff on the two separate approval pathways (partial-onset vs. generalized tonic-clonic) with their different combination therapy requirements. Failure to obtain prior authorization before dispensing will result in claim denials for Medicare Advantage members.