Denileukin diftitox
Denileukin diftitox (trade name Ontak) was an antineoplastic agent, an engineered protein combining Interleukin-2 and Diphtheria toxin. Denileukin diftitox could bind to Interleukin-2 receptors[1] and introduce the diphtheria toxin into cells that express those receptors, killing the cells. In some Leukemias and Lymphomas malignant cells express these receptors, so denileukin diftitox can target these.
| Clinical data | |
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| Trade names | Ontak |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a611024 |
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| Routes of administration | Intravenous |
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| Pharmacokinetic data | |
| Elimination half-life | 70-80 min |
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IUPAC name
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| Formula | C2560H4042N678O799S17 |
| Molar mass | 57647.3 g/mol g·mol−1 |
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In 1999 Ontak was approved by the U.S. Food and Drug Administration (FDA) for treatment of Cutaneous T-cell lymphoma (CTCL).[2]
There is some evidence tying it to vision loss and in 2006 the FDA added a black box warning to the drug's label.[2]
In 2014 marketing of Ontak was discontinued in the US.[3]
References
- Turturro F (2007). "Denileukin diftitox: a biotherapeutic paradigm shift in the treatment of lymphoid-derived disorders". Expert Rev Anticancer Ther. 7 (1): 11–7. doi:10.1586/14737140.7.1.11. PMID 17187516.
- FDA Page Last Updated: May 11, 2009 Changes in the Ontak (denileukin diftitiox) Package Insert to Include a Description of Ophthalmologic Adverse Events
- "FDA Drug Shortages". FDA. 31 January 2014. Retrieved 3 July 2017.
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