PEDIATRIC HYDROXYUREA STUDY IN SICKLE CELL DISEASE

$0M01FY2000RRNIH

University Of North Carolina Chapel Hill, Chapel Hill NC

Investigators

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Abstract

The purpose of this study is to determine: 1) If hydroxyurea is effective in increasing the level of fetal hemoglobin in children with sickle cell disease, 2) If there are serious toxicities (side effects) in children treated with this drug and, 3) If hydroxyurea will effect growth.

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