Mountain State Medical Policy Bulletin |
Section: | Injections |
Number: | I-85 |
Topic: | Natalizumab (Tysabri®) |
Effective Date: | January 1, 2008 |
Issued Date: | December 31, 2007 |
Date Last Reviewed: | 11/2007 |
Indications and Limitations of Coverage
Natalizumab (Tysabri®) is a monoclonal antibody indicated as monotherapy for the treatment of patients with relapsing forms of multiple sclerosis to delay the accumulation of physical disability and reduce the frequency of clinical exacerbations. The safety and efficacy of natalizumab beyond two years are unknown. Because natalizumab increases the risk of progressive multifocal leukoencephalopathy (PML), an opportunistic viral infection of the brain that usually leads to death or severe disability, natalizumab is generally recommended for patients who have had an inadequate response to, or are unable to tolerate, alternate multiple sclerosis therapies. Natalizumab has not been studied in patients with severe, disabling multiple sclerosis. The two main studies that appear in the FDA approved labeling only evaluated patients who had mild to moderate disability (Kurtzke Expanded Disability Status Scale scores between 0 and 5.0). Refer to the Text Attachment below for scale. Natalizumab will be covered when all the following criteria are met:
Safety and efficacy in treating patients with a diagnosis of anything other than the relapsing forms of multiple sclerosis (chronic progressive multiple sclerosis, Crohn's disease, etc.) or the use of natalizumab in combination with any other drug therapy for multiple sclerosis have not been established and will not be covered. The use of natalizumab for any other diagnosis not listed in the coverage criteria above is considered experimental/investigational, and therefore, not covered. A participating, preferred, or network provider can bill the member for the denied service. Coverage for natalizumab is determined according to individual or group customer benefits. Natalizumab is not reimbursable under the prescription drug benefit. |
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J2323 |
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 life-threatening condition and when medically necessary and appropriate for the patient’s condition. |
Rating Neurologic Impairment in Multiple Sclerosis: An Expanded Disability Status Scale (EDSS), Neurology, Vol. 33, No. 11, 11/1983 A Controlled Trial of Natalizumab for Relapsing Multiple Sclerosis, The New England Journal of Medicine, Vol. 348, No. 1, 01/2003 Tysabri® (Natalizumab) drug label; Biogen Idec, Inc., Cambridge, MA, 06/2006 Progressive Multifocal Leukoencephalopathy After Natalizumab Therapy for Crohn's Disease, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 Progressive Multifocal Leukoencephalopathy Complicating Treatment with Natalizumab and Interferon Beta -1a for Multiple Sclerosis, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 Progressive Multifocal Leukoencephalopathy in a Patient Treated with Natalizumab, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 Progressive Multifocal Leukoencephalopathy and Natalizumab - Unforeseen Consequences, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 Natalizumab and Progressive Multifocal Leukoencephalopathy, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 Evaluation of Patients Treated with Natalizumab for Progressive Multifocal Leukoencephalopathy, The New England Journal of Medicine, Vol. 353, No. 4, 07/2005 |
[Version 002 of I-85] |
[Version 001 of I-85] |
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