Onfi (clobazam), Sympazan (clobazam)

Indications for Prior Authorization

Onfi (clobazam) tablets and oral suspension, Sympazan (clobazam) oral film
  • For diagnosis of Lennox-Gastaut syndrome (LGS)
    Indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older.

  • For diagnosis of Refractory Seizures
    There is some clinical evidence to support the use in refractory seizures.

Criteria

Generic clobazam

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following:
    • Diagnosis of seizures associated with Lennox-Gastaut syndrome (LGS)
    • AND
    • Used as adjunctive therapy [A]
    • AND
    • Patient is 2 years of age or older
    • AND
    • Prescribed by or in consultation with a neurologist
    OR
  • All of the following: [4]
    • Diagnosis of seizures associated with Dravet syndrome (DS)
    • AND
    • Used in combination with Diacomit (stiripentol)
    • AND
    • Both of the following:
      • Patient is 6 months of age or older
      • Patient weighs greater than or equal to 7 kg
      AND
    • Prescribed by or in consultation with a neurologist
Generic clobazam [off label]

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following: [B, 5-6]
    • Diagnosis of refractory seizures (inadequate response to at least two antiepileptic drugs)
    • AND
    • Used as adjunctive therapy
    • AND
    • Prescribed by or in consultation with a neurologist
Brand Onfi

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following:
    • Diagnosis of seizures associated with Lennox-Gastaut syndrome (LGS)
    • AND
    • Used as adjunctive therapy [A]
    • AND
    • Patient is 2 years of age or older
    • AND
    • Prescribed by or in consultation with a neurologist
    • AND
    • Trial and failure or intolerance to generic clobazam tablets or oral suspension
    OR
  • All of the following: [4]
    • Diagnosis of seizures associated with Dravet syndrome (DS)
    • AND
    • Used in combination with Diacomit (stiripentol)
    • AND
    • Both of the following:
      • Patient is 6 months of age or older
      • Patient weighs greater than or equal to 7 kg
      AND
    • Prescribed by or in consultation with a neurologist
    • AND
    • Trial and failure or intolerance to generic clobazam tablets or oral suspension
Brand Onfi [off label]

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following: [B, 5-6]
    • Diagnosis of refractory seizures (inadequate response to at least two antiepileptic drugs)
    • AND
    • Used as adjunctive therapy
    • AND
    • Trial and failure or intolerance to generic clobazam tablets or oral suspension
    • AND
    • Prescribed by or in consultation with a neurologist
Sympazan

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following:
    • Diagnosis of seizures associated with Lennox-Gastaut syndrome (LGS)
    • AND
    • Used as adjunctive therapy [A]
    • AND
    • Patient is 2 years of age or older
    • AND
    • Prescribed by or in consultation with a neurologist
    • AND
    • One of the following:
      • Trial and failure or intolerance to generic clobazam tablets or oral suspension
      • For continuation of prior therapy
    OR
  • All of the following: [4]
    • Diagnosis of seizures associated with Dravet syndrome (DS)
    • AND
    • Used in combination with Diacomit (stiripentol)
    • AND
    • Both of the following:
      • Patient is 6 months of age or older
      • Patient weighs greater than or equal to 7 kg
      AND
    • Prescribed by or in consultation with a neurologist
    • AND
    • One of the following:
      • Trial and failure or intolerance to generic clobazam tablets or oral suspension
      • For continuation of prior therapy
Sympazan [off label]

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • All of the following: [B, 5-6]
    • Diagnosis of refractory seizures (inadequate response to at least two antiepileptic drugs)
    • AND
    • Used as adjunctive therapy
    • AND
    • Prescribed by or in consultation with a neurologist
    • AND
    • One of the following:
      • Trial and failure or intolerance to generic clobazam tablets or oral suspension
      • For continuation of prior therapy
Generic clobazam, Brand Onfi, or Sympazan

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)

  • Patient demonstrates positive clinical response to therapy
P & T Revisions

2024-06-17, 2024-01-04, 2023-10-03, 2023-04-24, 2023-01-14, 2022-01-07, 2021-09-28, 2021-05-21, 2021-01-05, 2019-12-12, 2019-10-29

  1. Onfi Prescribing Information. Lundbeck. Deerfield, IL. January 2023.
  2. Ng Y-T, Conry JA, Drummond R, et al. Randomized, phase III study results of clobazam in Lennox-Gastaut syndrome. Neurology. 2011;77:1473-81.
  3. Sympazan Prescribing Information. Aquestive Therapeutics. Warren, NJ. January 2023.
  4. Diacomit Prescribing Information. Biocodex. Beauvais, France. July 2022.
  5. Drislane, F. UptoDate. Refractory status epilepticus in adults. March 2023. Available at: https://www.uptodate.com/contents/refractory-status-epilepticus-in-adults?search=onfi&source=search_result&selectedTitle=3~17&usage_type=default&display_rank=3. Accessed April 18, 2023.
  6. Epilepsy Foundation. Drug Resistant Epilepsy. Available at: https://www.epilepsy.com/treatment/medicines/drug-resistant-epilepsy. Accessed April 18, 2023.

  • 2024-06-17: Removal of COT for Brand Onfi
  • 2024-01-04: Annual Review - No criteria changes
  • 2023-10-03: Program update to standard reauthorization language. No changes to clinical intent
  • 2023-04-24: Update guideline
  • 2023-01-14: Annual review - update to age/weight requirements for Dravet Syndrome
  • 2022-01-07: 2022 Annual Review
  • 2021-09-28: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-05-21: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-01-05: 2021 Annual Review. Removed reference to drug name from reauth criteria.
  • 2019-12-12: 2020 Annual Review, no changes to criteria.
  • 2019-10-29: Added step through generic for brand

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