Tositumomab
From Wikipedia, the free encyclopedia
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Tositumomab?
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| Therapeutic monoclonal antibody | |
| Source | Mouse |
| Target | CD20 |
| Identifiers | |
| CAS number | |
| ATC code | V10 |
| PubChem | ? |
| DrugBank | |
| Chemical data | |
| Formula | C6416H9874N1688O1987S44 |
| Mol. mass | 143859.7 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
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| Legal status | |
| Routes | ? |
Tositumomab is a monoclonal antibody derived from immortalized mouse cells. It is a IgG2a anti-CD20 antibody and is covalently bound to 131I. 131I emits both beta and gamma radiation and decays with a half-life of 8 days.
Clinical trials have established the efficacy of tositumomab in patients with relapsed or chemotherapy/rituxan refractory follicular lymphoma.
The drug was developed by Dr. Mark Kaminski and Dr. Richard Wahl. It is manufactured by Corixa. It sells in the U.S. under the trade name Bexxar.
There is some evidence that it may cause a smaller decrease in platelet counts than ibritumomab tiuxetan does.[1]
[edit] References
- ^ Jacene HA, Filice R, Kasecamp W, Wahl RL (2007). "Comparison of 90Y-ibritumomab tiuxetan and 131I-tositumomab in clinical practice". J. Nucl. Med. 48 (11): 1767–76. doi:. PMID 17942813.
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