This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The objective of this study is to compare the effects of ica-17043 to placebo with or without hydroxyurea (an oral drug used for treatment of sickle cell disease) in patients wiht sickle cell disease who have had 2 or more acute sickle-related painful crisise requiring a visit to a medical facility within the past 12 monts. Additional purposes are to obtain further safety information on the chronic dosing of ica-17043 and to find out how much ica-17043 is in the blood following chronic dosing.
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