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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Specialty Quantity Limit Rinvoq 3175-H P2023b

Drug
RINVOQ  (upadacitinib)


Policy:

I.  PROGRAM DESCRIPTION

The standard limit is designed to allow a quantity sufficient for the most common uses of the medication. If the member’s plan allows a quantity limit exception review for the requested medication, coverage of an additional quantity may be provided up to the exception limit with prior authorization.


II.  COVERED QUANTITIES

 Medication

 Standard Limit

 Exception Limit*

 FDA-recommended dosing

  Rinvoq (upadacitinib)
  15 mg extended-
  release tablet

  30 tablets
  per 30 days

 

  N/A

  RA, PsA, AS, nr-axSpA: 15 mg once daily

  Atopic dermatitis
  •  Pediatric patients 12 years of age and
     older weighing at least 40 kg and adults
     less than 65 years of age:
     º  Initiate treatment with 15 mg once
        daily. A dosage of 30 mg once daily
        may be considered if an adequate
        response is not achieved.
  •  Dose adjustments: Reduce to 15 mg
     once daily for patients:
     º  65 years of age and older
     º  With severe renal impairment (not
         recommended for patients with end
         stage renal disease)
     º  Receiving strong CYP3A4 inhibitors

 Ulcerative colitis
  •  Induction dose of 45 mg once daily for 8
     weeks
  •  Maintenance dose of 15 mg once daily. A
     dosage of 30 mg once daily may be
     considered for patients with refractory,
     severe or extensive disease.
  •  Dose adjustments: Induction dose of 30
     mg once daily for 8 weeks and
     maintenance dose of 15 mg once daily for
     patients:
     º  With severe renal impairment
     º  With mild to moderate hepatic
         impairment (Child-Pugh A or B)
     º  Receiving strong CYP3A4 inhibitors

 Crohn’s disease
  •  Induction dose of 45 mg once daily for
     12 weeks
  •  Maintenance dose of 15 mg once daily.
      A dosage of 30 mg once daily may be
      considered for patients with refractory,
      severe or extensive disease
  •  Dose adjustments: Induction dose of 30
      mg once daily for 12 weeks and
     maintenance dose of 15 mg once daily for
     patients:
     º  With severe renal impairment
     º  With mild to moderate hepatic
         impairment (Child-Pugh A or B)
     º  Receiving strong CYP3A4 inhibitors

  Rinvoq (upadacitinib)
  30 mg extended-
  release tablet

  30 tablets
  per 30 days

  N/A

  Rinvoq (upadacitinib)
  45 mg extended-
  release tablet

  No standard limit
  - only used for
  induction dosing

 

 

 

 

 

 

 

 

 

  84 tablets
  per 84 days

  Abbreviations: RA = rheumatoid arthritis, PsA = psoriatic arthritis; AS = ankylosing spondylitis; nr-axSpA = non-radiographic axial spondyloarthritis
  *Coverage up to the exception limits may be provided with prior authorization via the Specialty Post Limit Quantity
  Exception Criteria for approval.

 


Place of Service:

Outpatient

The above policy is based on the following references:
  1. Rinvoq [package insert]. North Chicago, IL: AbbVie Inc.; June 2023.
Copyright Aetna Inc. All rights reserved. Pharmacy Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.

December 09, 2023
Aetna
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