Abstract
Despite the successes of deferoxamine (DFO) in the treatment and prevention of iron overload, an effective orally available iron chelating drug is needed, since erratic compliance with irritating, cumbersome parenteral infusions still results in fatal iron accumulation in many patients. Disorders of increased iron absorption should also benefit from the development of safe and effective iron chelating agents. Individuals with non-transfusion-dependent thalassemia (thalassemia 'intermedia'), exhibit excessive dietary iron absorption that can lead to serious iron loading by the second or third decade of life. An orally effective iron-chelating drug would have major therapeutic advantages for all these patients.
Original language | English |
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Pages (from-to) | 9-11 |
Number of pages | 3 |
Journal | Bone Marrow Transplantation |
Volume | 12 |
Issue number | SUPPL. 1 |
State | Published - 1993 |
Externally published | Yes |