Viewing Study NCT00119457



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00119457
Status: COMPLETED
Last Update Posted: 2009-06-03
First Post: 2005-07-05

Brief Title: Factor IX Inhibition in Thrombosis Prevention The FIXIT Trial
Sponsor: vTv Therapeutics
Organization: vTv Therapeutics

Study Overview

Official Title: A Multi-Center Placebo-Controlled Evaluation of the Safety and Efficacy of Three Weeks Extended VTE Prophylaxis With Daily Oral Doses of TTP889 After One Week of Standard Prophylactic Treatment Following Hip Fracture Surgery
Status: COMPLETED
Status Verified Date: 2009-06
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 determine whether TTP889 prevents venous thromboembolism following surgery to repair hip fracture
Detailed Description: FIXIT is the first Phase 2 study of TTP889 The trial is a proof-of-concept study to determine the safety and antithrombotic efficacy of TTP889 in patients at risk for venous thromboembolism VTE The study is a multi-center randomized double-blind parallel-group evaluation of 300 mg TTP889 or placebo administered orally once daily for three weeks in patients who have undergone surgery to repair unilateral fracture of the upper third of either femur and who have completed 5 to 9 days of postoperative prophylactic treatment for VTE

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
Eudract CT2004-002511-83 None None None