Viewing Study NCT00122304



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00122304
Status: COMPLETED
Last Update Posted: 2007-02-21
First Post: 2005-07-19

Brief Title: Study of Safety in Hemolytic Paroxysmal Nocturnal Hemoglobinuria PNH Patients Treated With Eculizumab
Sponsor: Alexion Pharmaceuticals Inc
Organization: Alexion Pharmaceuticals Inc

Study Overview

Official Title: Safety in Hemolytic PNH Patients Treated With Eculizumab a Multi-Center Open-Label Research Design Study
Status: COMPLETED
Status Verified Date: 2007-02
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 primary objective is to evaluate the safety of eculizumab in patients with transfusion-dependent hemolytic PNH
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
Secondary IDs
Secondary ID Type Domain Link
C04-002 None None None