Study Evaluating The Safety Of Xyntha In Usual Care Settings

Status Terminated

Clinical Trial Summary

The purpose of this study is to collect safety information associated with the use of Xyntha in a usual care setting. Upon meeting eligibility criteria, patients will be required to have approximately 5 study visits over a 2 year period. Procedures completed throughout the study include collection of vital signs, physical exams, and laboratory assessments. Patients will be required to complete an infusion log for each Xyntha infusion.

Clinical Trial Description

The study was terminated on May 12, 2011 due to poor enrollment prospects and the study's similarity to another ongoing trial with ReFacto AF.

The termination of this study has no impact on subject safety or well being. The decision to terminate the trial was not based on any safety concerns. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Hemophilia A

Clinical Trial Details

NCT number	NCT00765726
Study type	Interventional
Source	Pfizer
Contact
Status	Terminated
Phase	Phase 4
Start date	February 2009
Completion date	August 2011

View Details

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