Vyjuvek (beremagene geperpavec-svdt)

Indications for Prior Authorization

Vyjuvek (beremagene geperpavec-svdt)
  • For diagnosis of Wound care in dystrophic epidermolysis bullosa
    Indicated for the treatment of wounds in patients 6 months of age and older with dystrophic epidermolysis bullosa (DEB) with mutation(s) in the collagen type VII alpha 1 chain (COL7A1) gene.

Criteria

Vyjuvek

Prior Authorization (Initial Authorization)

Length of Approval: 6 Month(s)

  • Diagnosis of dystrophic epidermolysis bullosa (DEB)
  • AND
  • Patient has mutation(s) in the collagen type VII alpha 1 chain (COL7A1) gene
  • AND
  • Medication is being used for the treatment of wounds that require healing
  • AND
  • Patient is 6 months of age or older
  • AND
  • Medication will be applied by a healthcare professional
  • AND
  • Wound(s) being treated meet all of the following criteria [2]:
    • Adequate granulation tissue
    • Excellent vascularization
    • No evidence of active wound infection in the wound being treated
    • No evidence or history of squamous cell carcinoma in the wound being treated
    AND
  • Medication is not being used concurrently with other FDA approved therapies (e.g., Filsuvez) on the same target wound for the treatment of epidermolysis bullosa
  • AND
  • Standard wound care management not adequate in healing wounds (e.g., daily wound dressings, pain management, controlling infections)
  • AND
  • Prescribed by or in consultation with a specialist with expertise in wound care
Vyjuvek

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)

  • Patient demonstrates positive clinical response to therapy as evidenced by wound healing (e.g., reduction in number or size of wounds)
  • AND
  • Wound(s) being treated meet all of the following criteria [2]:
    • Adequate granulation tissue
    • Excellent vascularization
    • No evidence of active wound infection in the wound being treated
    • No evidence or history of squamous cell carcinoma in the wound being treated
    AND
  • Medication is not being used concurrently with other FDA approved therapies (e.g., Filsuvez) on the same target wound for the treatment of epidermolysis bullosa
  • AND
  • Prescribed by or in consultation with a specialist with expertise in wound care
P & T Revisions

2024-07-03, 2024-05-20, 2024-03-13, 2023-07-28, 2023-08-17

  1. Vyjuvek Prescribing Information. Krystal Biotech, Inc. Pittsburgh, PA. May 2023.
  2. Guide SV, Gonzalez ME, Bağcı IS, et al. Trial of beremagene geperpavec (B-VEC) for dystrophic epidermolysis bullosa. N Engl J Med 2022;387:2211-9. DOI: 10.1056/NEJMoa2206663

  • 2024-07-03: 2024 UM Annual Review. No criteria changes
  • 2024-05-20: update guideline
  • 2024-03-13: Changed specialist prescriber from dermatologist to specialist with expertise in wound care
  • 2023-07-28: New program for Vyjuvek
  • 2023-08-17: New program for Vyjuvek