Subject: Vimizim 2057-A SGM P2024
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VIMIZIM
(elosulfase alfa)
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Policy:
I. INDICATIONS
The indications below including FDA-approved indications and compendial uses are
considered a covered benefit provided that all the approval criteria are met and the member
has no exclusions to the prescribed therapy.
FDA-Approved Indication
Vimizim is indicated for patients with Mucopolysaccharidosis type IVA (MPS IVA, Morquio A
syndrome).
All other indications are considered experimental/investigational and not medically necessary.
II. DOCUMENTATION
Submission of the following information is necessary to initiate the prior authorization review:
A. Initial requests: N-acetylgalactosamine-6-sulfatase enzyme assay or genetic testing results
supporting diagnosis.
B. Continuation requests: chart notes documenting a clinically positive response to therapy,
which shall include improvement, stabilization, or slowing of disease progression.
III. CRITERIA FOR INITIAL APPROVAL
Mucopolysaccharidosis IVA (MPS IVA, Morquio A syndrome)
Authorization of 12 months may be granted for treatment of MPS IVA (Morquio A syndrome)
when the diagnosis of MPS IVA was confirmed by enzyme assay demonstrating a deficiency of
N-acetylgalactosamine-6-sulfatase enzyme activity or by genetic testing.
IV. CONTINUATION OF THERAPY
Authorization of 12 months may be granted for continued treatment in members requesting
reauthorization for an indication listed in Section III who have a clinically positive response to
therapy, which shall include improvement, stabilization, or slowing of disease progression.
Place of Service:
Outpatient
The above policy is based on the following references:
- Vimizim [package insert]. Novato, CA: BioMarin Pharmaceutical Inc.; December 2019.
- Hendriksz CJ, Berger KI, Giugliani R, et al. International guidelines for the management and treatment of Morquio A syndrome. Am J Med Genet A. 2015;167A(1):11-25.
- Clinical Consult: CVS Caremark Clinical Programs Review. Focus on Enzyme Disorders. April 2021.
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.
June 16, 2024