Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | I-55-017 |
Topic: | Agalsidase beta (Fabrazyme) |
Section: | Injections |
Effective Date: | May 28, 2018 |
Issue Date: | May 28, 2018 |
Last Reviewed: | February 2018 |
Agalsidase beta (Fabrazyme®) serves as an exogenous source of the lysosomal enzyme α-glucosidase A (a-GalA), catalyzing the hydrosis of glycosphinogolipids, including globotriaosylceramide (GL-3), hence reducing its deposition in capillary endothelium of the kidney, heart, brain and other tissue types. α-glucosidase A deficiency, otherwise known as Fabry Disease, is an X- linked genetic disorder of glycosphingolipid metabolism. Deficiency of a-Gal leads to progressive accumulation of glycoshingolipids, predominantly GL-3, in many body tissues, occurring over a period of years. Clinical manifestations of the disease include renal failure, cardiomyopathy and cerebrovascular accidents. |
This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.
Policy Position Coverage is subject to the specific terms of the member’s benefit plan. |
Aglasidas beta (Fabrazyme) may be considered medically necessary for the treatment of Fabry disease when ALL of the following criteria are met:
Aglasidas beta (Fabrazyme) for any other indication is considered experimental/investigational, and therefore, non-covered.
Agalsidase beta (Fabrazyme) is not reimbursable under the prescription drug benefit.
NOTE: Dosage recommendations per the FDA label.
Place of Service: Outpatient |
Experimental/Investigational (E/I) services are not covered regardless of place of service.
The policy position applies to all commercial lines of business |
Denial Statements |
Services that do not meet the criteria of this policy will be considered experimental/investigational (E/I). A network provider can bill the member for the experimental/investigational service. The provider must give advance written notice informing the member that the service has been deemed E/I. The member must be provided with an estimate of the cost and the member must agree in writing to assume financial responsibility in advance of receiving the service. The signed agreement must be maintained in the provider’s records.
Links |
7/2017 Revised criteria for Agalsidase beta (Fabrazyme®)
1/2018, Criteria Revised for Agalsidase beta (Fabrazyme)