Viewing Study NCT01301898



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Last Modification Date: 2024-10-26 @ 10:32 AM
Study NCT ID: NCT01301898
Status: COMPLETED
Last Update Posted: 2012-02-14
First Post: 2011-02-22

Brief Title: To Evaluate the Safety and Efficacy of GC1111 Recombinant Human Iduronate-2-sulfatase in Hunter Syndrome Patients
Sponsor: Green Cross Corporation
Organization: GC Biopharma Corp

Study Overview

Official Title: Randomized Single-blind Active-controlled Phase 12 Study to Evaluate the Safety and Efficacy of GC1111 Recombinant Human Iduronate-2-sulfatase in Hunter Syndrome Mucopolysaccharidosis II Patients
Status: COMPLETED
Status Verified Date: 2012-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the safety and efficacy of GC1111 recombinant human iduronate-w-sulfatase in Hunter Syndrome Mucopolysaccharidosis II patients
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