Viewing Study NCT00048620



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00048620
Status: COMPLETED
Last Update Posted: 2006-11-03
First Post: 2002-11-04

Brief Title: Study of Recombinant Human N-Acetylgalactosamine 4-Sulfatase in Patients With MPS VI
Sponsor: BioMarin Pharmaceutical
Organization: BioMarin Pharmaceutical

Study Overview

Official Title: Double-Blind2 Dose Group Study of Recombinant Human N-Acetylgalactosamine 4-Sulfatase in Patients With MPS VI
Status: COMPLETED
Status Verified Date: 2006-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of the study is to evaluate the safety efficacy and pharmacokinetics of two dose levels of weekly intravenous infusions of recombinant human N-acetylgalactosamine 4-sulfatase rhASB for a minimum of 24 weeks in patients diagnosed with MPS VI
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None