Item |
Information |
Drug Groups
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approved; investigational |
Description
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An anthracenedione-derived antineoplastic agent. [PubChem] |
Indication |
For the treatment of secondary (chronic) progressive, progressive relapsing, or worsening relapsing-remitting multiple sclerosis |
Pharmacology |
Mitoxantrone has been shown in vitro to inhibit B cell, T cell, and macrophage proliferation and impair antigen presentation, as well as the secretion of interferon gamma, TNFa, and IL-2. |
Toxicity |
Severe leukopenia with infection. |
Affected Organisms |
• |
Humans and other mammals |
|
Biotransformation |
Hepatic |
Absorption |
Poorly absorbed following oral administration |
Half Life |
75 hours |
Protein Binding |
78% |
Distribution |
* 1000 L/m2 |
Clearance |
* 21.3 L/hr/m2 [Elderly patients with breast cancer receiving IV administration of 15-90 mg/m2] * 28.3 L/hr/m2 [Non-elderly patients with nasopharyngeal carcinoma receiving IV administration of 15-90 mg/m2] * 16.2 L/hr/m2 [Non-elderly patients with malignant lymphoma receiving IV administration of 15-90 mg/m2] |
References |
• |
Fox EJ: Management of worsening multiple sclerosis with mitoxantrone: a review. Clin Ther. 2006 Apr;28(4):461-74.
[Pubmed]
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External Links |
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