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tapinarof cream 1 %Blue Cross Blue Shield of Texas

plaque psoriasis

Initial criteria

  • ONE of the following:
  • A. Diagnosis of plaque psoriasis AND BOTH of the following:
  • 1. Affected body surface area (BSA) ≤ 20% AND
  • 2. ONE of the following:
  • A. Tried and had an inadequate response to a topical corticosteroid or topical calcineurin inhibitor used in the treatment of plaque psoriasis after at least a 2-week duration of therapy OR
  • B. Intolerance or hypersensitivity to therapy with topical corticosteroids or topical calcineurin inhibitors used in the treatment of plaque psoriasis OR
  • C. FDA labeled contraindication to ALL topical corticosteroids and ALL topical calcineurin inhibitors used in the treatment of plaque psoriasis
  • B. Diagnosis of atopic dermatitis (AD) AND BOTH of the following:
  • 1. ONE of the following:
  • A. Tried and had an inadequate response to at least a low-potency topical corticosteroid or topical calcineurin inhibitor or topical emollients used in treatment of AD after at least a 4-week duration of therapy OR
  • B. Intolerance or hypersensitivity to therapy with low-potency topical corticosteroid or topical calcineurin inhibitor used in treatment of AD OR
  • C. FDA labeled contraindication to ALL low-potency topical corticosteroid or topical calcineurin inhibitor used in treatment of AD AND
  • 2. BOTH of the following:
  • A. Patient is currently treated with topical emollients and practicing good skin care AND
  • B. Patient will continue the use of topical emollients and good skin care practices in combination with the requested agent
  • C. Another FDA labeled indication for the requested agent and route of administration
  • If patient has an FDA labeled indication, then ONE of the following:
  • A. Age is within FDA labeling for the requested indication for the requested agent OR
  • B. Support for using the requested agent for the patient's age for the requested indication
  • Prescriber is a specialist in the area of the patient’s diagnosis (e.g., dermatologist) or has consulted with a specialist in the area of the patient’s diagnosis
  • Patient does NOT have any FDA labeled contraindications to the requested agent

Reauthorization criteria

  • Patient has been previously approved for the requested agent through the plan’s Prior Authorization process
  • Patient has had clinical benefit with the requested agent
  • Prescriber is a specialist in the area of the patient’s diagnosis (e.g., dermatologist) or has consulted with a specialist in the area of the patient’s diagnosis
  • Patient does NOT have any FDA labeled contraindications to the requested agent

Approval duration

12 months