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 primary objective of this clinical trial is to determine the efficacy of enzyme replacement therapy with idursulfase (DRX006A) in the treatment of patients with Mucopolysaccharidosis Type II (MPS II or Hunter Syndrome) as compared to placebo. Idursulfase will be administered as a weekly infusion at a dose of 0.5 mg/kg. The secondary objectives of the study include 1. The determination of the efficacy of an eveyr other week regimen of idursulfase given at the same 0.5 mg/kg dose and 2. The evaluation of the safety and tolerability of the 2 dosing regimens of idursulfase therapy in a large MPS II patient population.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000188-42
Application #
7375033
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2005-12-01
Project End
2006-11-30
Budget Start
2005-12-01
Budget End
2006-11-30
Support Year
42
Fiscal Year
2006
Total Cost
$12,097
Indirect Cost
Name
Baylor College of Medicine
Department
Pediatrics
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
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