Mountain State Medical Policy Bulletin |
Section: | Injections |
Number: | I-9 |
Topic: | Ceredase/Cerezyme Injections |
Effective Date: | August 1, 2005 |
Issued Date: | May 12, 2008 |
Date Last Reviewed: | 08/2005 |
Indications and Limitations of Coverage
Ceredase-J0205 and cerezyme (imiglucerase)-J1785 are drugs indicated for use as an enzyme replacement therapy for patients with a confirmed diagnosis and exhibiting signs and symptoms of Type I (adult) Gauchers disease (lipid metabolism disorder). Coverage for therapeutic injections is determined according to individual or group customer benefits. Ceredase and cerezyme are indicated for treatment when one or more of the following conditions exists in patients with Type I Gauchers disease:
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J0205 | J1785 |
Under the Federal Employee Program, all services that utilize FDA-approved drugs, devices, or biological products are eligible when intended for the treatment of a serious or life-threatening condition and when medically necessary and appropriate for the patient's condition. |
Management of Neutralizing Antibody to Ceredase in a Patient with Type 3 Gaucher Disease, Pediatrics, Official Journal of the American Academy of Pediatrics, Vol. 100, No. 5, 12/1997 Gaucher Disease: Recommendations on Diagnosis, Evaluation, and Monitoring, Archives Internal Medicine, Vol. 158, No. 16, 09/1998 Cardiac Response to Enzyme-Replacement Therapy in Gaucher's Disease, The New England Journal of Medicine, Vol. 339, No. 16, 10/1998 Cessation of Enzyme Replacement Therapy in Gaucher Disease, Genetic Medicine, Vol. 4, No. 6, 11/2002 Ceredase® (alglucerase injection) drug label, Genzyme Corporation, Cambridge, MA, 10/2004 Cerezyme® (imiglucerase for injection) drug label, Genzyme Corporation, Cambridge, MA, 04/2005 Superior Effects of High-Dose Enzyme Replacement Therapy in Type I Gaucher Disease on Bone Marrow Involvement and Chitotriosidase Levels: A 2 Center Retrospective Analysis, Blood, Vol. 108, No. 3, 08/2006 The Clinical and Demographic Characteristics of Non-neuronopathic Gaucher Disease in 887 Children at Diagnosis, Archives of Pediatrics & Adolescent Medicine, Vol. 16, No. 6, 10/2006 Low-dose Therapy Trumps High-dose Therapy Again in the Treatment of Gaucher Disease, Blood, Vol. 108, No. 3, 08/2006 Prevalance and Transmission of Gaucher Disease, Accessed May 2, 2008. National Gaucher Foundation, Rockville, MD |
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