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Chemical, Pharmacological, Toxicological and Therapeutic Advances of Deferiprone (L1) and Other Iron and Aluminium Chelators

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Toxicology - From Cells to Man

Part of the book series: Archives of Toxicology ((TOXICOLOGY,volume 18))

Abstract

A global breakthrough in oral chelation therapy with the a-ketohydroxypyridine chelating drug l,2-dimethyl-3-hydroxypyrid-4-one (LI, INN/BAN: Deferiprone) (Kontoghiorghes 1982) in iron and aluminium overloaded patients has recently been achieved. Since the initiation of clinical trials with LI in 1987 and prior to its recent registration in India, over 800 patients with ten different conditions in 16 countries have received it, in some cases daily for over 6 years. The major toxic side effects, which all appear to be reversible, include agranulocytosis, musculoskeletal and joint pains, zinc deficiency and gastric intolerance. Oral LI appears to be as effective as subcutaneous desferoxamine (DF) in iron and aluminium removal and has low toxicity. Other α-ketohydroxypyridines are also currently being developed.

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© 1996 Springer-Verlag Berlin Heidelberg

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Kontoghiorghes, G.J. (1996). Chemical, Pharmacological, Toxicological and Therapeutic Advances of Deferiprone (L1) and Other Iron and Aluminium Chelators. In: Seiler, J.P., Kroftová, O., Eybl, V. (eds) Toxicology - From Cells to Man. Archives of Toxicology, vol 18. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-61105-6_21

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  • DOI: https://doi.org/10.1007/978-3-642-61105-6_21

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-64696-6

  • Online ISBN: 978-3-642-61105-6

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