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SunosiCareFirst (Caremark)

Excessive daytime sleepiness associated with narcolepsy

Preferred products

  • armodafinil
  • modafinil

Initial criteria

  • The requested drug is being prescribed by, or in consultation with, a sleep specialist.
  • The diagnosis has been confirmed by sleep study.
  • The patient meets ONE of the following:
  • • The patient has experienced an inadequate treatment response to armodafinil OR modafinil.
  • • The patient has experienced an intolerance to armodafinil OR modafinil.
  • • The patient has a contraindication that would prohibit a trial of ALL of the following: armodafinil, modafinil.

Reauthorization criteria

  • The patient has achieved or maintained a decrease in daytime sleepiness with narcolepsy from baseline.

Approval duration

12 months