Viewing Study NCT01913405



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Last Modification Date: 2024-10-26 @ 11:10 AM
Study NCT ID: NCT01913405
Status: COMPLETED
Last Update Posted: 2021-05-24
First Post: 2013-06-27

Brief Title: Phase 3 Efficacy and Safety Study of BAX 855 in Severe Hemophilia A Patients Undergoing Surgical Procedures
Sponsor: Baxalta now part of Shire
Organization: Takeda

Study Overview

Official Title: A Phase 3 Multi-Center Open Label Study of Efficacy and Safety of PEGylated rFVIII BAX 855 in Previously Treated Patients With Severe Hemophilia A Undergoing Surgical or Other Invasive Procedures
Status: COMPLETED
Status Verified Date: 2021-04
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 the study is to evaluate the efficacy and safety of BAX 855 in severe hemophilia A previously treated PTP males 12 to 65 years of age who are undergoing elective surgical or other invasive procedures
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
2013-001359-11 EUDRACT_NUMBER None None